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FDA 510(k)

NOVO VIVO MODEL #17140 AND #17135

K-Number: K880377 · 1988-04-04

ApplicantGenesis Industries, Inc.
Decision Date1988-04-04
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NOVO VIVO MODEL #17140 AND #17135 is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Industries, Inc.. It received FDA 510(k) clearance on 1988-04-04 under 510(k) number K880377. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVO VIVO MODEL #17140 AND #17135?

NOVO VIVO MODEL #17140 AND #17135 is a medical device that received FDA 510(k) clearance on 1988-04-04. The listed applicant is Genesis Industries, Inc.. The 510(k) number is K880377.

When did NOVO VIVO MODEL #17140 AND #17135 receive FDA 510(k) clearance?

NOVO VIVO MODEL #17140 AND #17135 received FDA 510(k) clearance on 1988-04-04, under 510(k) number K880377.

Who is the listed applicant for NOVO VIVO MODEL #17140 AND #17135?

The FDA 510(k) record lists Genesis Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVO VIVO MODEL #17140 AND #17135?

The FDA product code for NOVO VIVO MODEL #17140 AND #17135 is GAA.

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Other records listing Genesis Industries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K994361ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELLK962828EVERT-ITK880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPK833287SATIN CAST ECONOCASTK833290C & B 40 PENTRO C & B40K833278C & B 45

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Related Devices (Code: GAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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