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

NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP

K Number: K880376 · Decision Feb 16, 1988
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
17
Review Days
20

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Basic Information

Device Name
NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP
K Number
K880376
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Genesis Industries, Inc.
Date Received
January 27, 1988
Decision Date
February 16, 1988
Product Code
GBS
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
GBS Catheter, Ventricular, General & Plastic Surgery

Similar 510(k) Clearances

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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
K880377 NOVO VIVO MODEL #17140 AND #17135
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. →