FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NOVO VIVO MODEL #17140 AND #17135

K Number: K880377 · Decision Apr 4, 1988
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
17
Review Days
68

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Basic Information

Device Name
NOVO VIVO MODEL #17140 AND #17135
K Number
K880377
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Genesis Industries, Inc.
Date Received
January 27, 1988
Decision Date
April 4, 1988
Product Code
GAA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GAA Needle, Aspiration And Injection, Disposable

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Other Clearances by Genesis Industries, Inc.

K Number Device Name
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
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
Search all 17 clearances from Genesis Industries, Inc. →