Genesis Industries, Inc.
FDA 510(k) medical device clearances.
Top product codes for Genesis Industries, Inc.
Recent clearances by Genesis Industries, Inc.
- K994361 — ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL
- K962828 — EVERT-IT
- K880377 — NOVO VIVO MODEL #17140 AND #17135
- K880376 — NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP
- K833287 — SATIN CAST ECONOCAST
- K833290 — C & B 40 PENTRO C & B40
- K833278 — C & B 45
- K833289 — C & B 61 PENTRON C & B61
- K833280 — SUPRA AP CHOICE 83
- K833285 — RX IV PENTRON IV
- K833288 — C & B57 PENTRON C & B57
- K833279 — NATURELLE-LITE
- K833281 — RX D PENTRON
- K833282 — RX NYSP PENTRON 60
- K833283 — RX ORY PENTRON C & B
- K833284 — RX 41 PENTRON 41
- K833286 — RX SEG ECONOPLUS
Data sourced from openFDA. This site is unofficial and independent of the FDA.