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

LAP SPONGES

K Number: K791872 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
6
Review Days
53

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Basic Information

Device Name
LAP SPONGES
K Number
K791872
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Carwild Corp.
Date Received
September 21, 1979
Decision Date
November 13, 1979
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EFQ), ordered by most recent decision date.

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Other Clearances by Carwild Corp.

K Number Device Name
K913303 LAP SPONGES, MODIFIED
K913302 DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED
K833688 SUTURE REMOVAL KITS STERILE
K791871 NEUROLOGICAL SPONGES (PATTIES)
K791870 DISPOSABLE SPECIALITY SPONGES