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

PMS ANGIO DRAPE

K Number: K890471 · Decision Feb 27, 1989
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
19
Review Days
27

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Basic Information

Device Name
PMS ANGIO DRAPE
K Number
K890471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Professional Medical Services
Date Received
January 31, 1989
Decision Date
February 27, 1989
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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K Number Device Name
K913094 DISPOSABLE SLIDE VALVE MANIFOLD
K910378 PRESSURE MONITORING EXTENSION LINE
K904508 CONDOR ANALOG INFLATION SYRINGE
K904954 CONDOR DIGITAL INFLATION SYRINGE
K902606 RADIOPAQUE RULER
K884577 PROCEDURE READY TRAYS
K884497 CONTROL SYRINGE
K872448 BLOOD CONTAINMENT PACK
K864555 3 RING ATTACHMENT
K854941 PMS PERCUTANEOUS PUNCTURE NEEDLE
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