Optimed Technologies, Inc.

15 FDA 510(k) medical device clearances.

Top product codes for Optimed Technologies, Inc.

INI — Physical Medicine 3 devices
HET — Obstetrics/Gynecology 2 devices
HIH — Obstetrics/Gynecology 2 devices
DQO — Cardiovascular 1 device
EOB — Ear, Nose, Throat 1 device
EOQ — Ear, Nose, Throat 1 device
FGA — Gastroenterology, Urology 1 device
GCM — Gastroenterology, Urology 1 device
HOX — Ophthalmic 1 device
HRX — Orthopedic 1 device

Recent clearances by Optimed Technologies, Inc.

K972520 — OPTIVIEW LLZ · 1997-09-29
K955274 — BOOSTER LITE 3 MOTORIZED SCOOTER INI · 1996-11-04
K955275 — BOOSTER TROPHY 5 MOTORIZED SCOOTER INI · 1996-11-04
K955276 — BOOSTER LITE 4 MOTORIZED SCOOTER INI · 1996-11-04
K943598 — FLEXIBLE FIBER OPTIC LAPAROSCOPES HET · 1994-10-18
K926597 — LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) HET · 1994-07-12
K921942 — HYSTEROSCOPE (AND ACCESSORIES) HIH · 1994-06-24
K922711 — FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE HIH · 1994-05-17
K921985 — ARTHROSCOPE & ACCESSORIES HRX · 1993-06-29
K922826 — FLEXIBLE FIBER OPTIC ENDOSCOPE FGA · 1993-02-19
K921883 — ENDOSCOPE GCM · 1992-11-23
K922937 — FLEXIBLE FIBER OPTIC ENDOSCOPE EOQ · 1992-09-14
K895245 — FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE EOB · 1989-11-17
K883337 — PL 20/20 INFANT VISION TESTER HOX · 1988-10-31
K880661 — FIBEROPTIC CATHETER DQO · 1988-05-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.