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

ZEISS DISPOSABLE, STERILE SURGICAL DRAPE

K Number: K800552 · Decision Mar 20, 1980
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
44
Review Days
10

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Basic Information

Device Name
ZEISS DISPOSABLE, STERILE SURGICAL DRAPE
K Number
K800552
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Carl Zeiss, Inc.
Date Received
March 10, 1980
Decision Date
March 20, 1980
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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K961380 CPC PROBE
K961171 HUMPHREY OCT SCANNER
K954167 HUMPHREY FIELD ANALYZER (HFA II)
K952894 VISULINK 900 ARGON
K950985 ZEISS ENDOLIVE STERO ENDOSCOPE
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