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

LAPAROTOMY SPOGNE

K Number: K772089 · Decision Nov 11, 1977
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
15
Review Days
7

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Basic Information

Device Name
LAPAROTOMY SPOGNE
K Number
K772089
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
General Medical Co.
Date Received
November 4, 1977
Decision Date
November 11, 1977
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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K900110 OPERAND* LUBRICATING JELLY
K853635 SUBDERM TM
K844652 C.A.S.E. CONTAINER
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K820689 C.S.R. WRAPPERS
K820521 STERILIZATION WRAP
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