FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SPONGE, LAPAROTOMY GAUZE

K Number: K760113 · Decision Jul 15, 1976
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
47
Review Days
21

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Basic Information

Device Name
SPONGE, LAPAROTOMY GAUZE
K Number
K760113
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Parke-Davis Co.
Date Received
June 24, 1976
Decision Date
July 15, 1976
Product Code
EFQ
Advisory Committee
Unknown
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
EFQ Gauze/Sponge, Internal

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