FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GOWN, SURGICAL, SURGINE

K Number: K770250 · Decision Mar 7, 1977
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
56
Review Days
27

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Basic Information

Device Name
GOWN, SURGICAL, SURGINE
K Number
K770250
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Surgikos, Inc.
Date Received
February 8, 1977
Decision Date
March 7, 1977
Product Code
BZQ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZQ Monitor, Breathing Frequency

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Other Clearances by Surgikos, Inc.

K Number Device Name
K875107 HEALTH CARE EYE PROTECTION
K874653 STERILE SURGICAL SCRUB BRUSH
K861441 NEUTRALON SURGICAL GLOVES
K852870 BARRIER SURGICAL GOWN
K822535 CIDEX*DIALYZER DISINFECTING SOLUTION
K820543 BARRIER ANTIMICROBIAL INCISE DRAPE
K820542 SURGIKOS INCISE DRAPE
K811871 BACTERICIDAL INCISE DRAPE
K810316 SURGIKOS FACE MASK
K801864 BARRIER APERTURED DRAPE
Search all 56 clearances from Surgikos, Inc. →