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

GUAZE SPONGES

K Number: K874067 · Decision Dec 14, 1987
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
11
Review Days
70

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Basic Information

Device Name
GUAZE SPONGES
K Number
K874067
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Interpro Intl., Inc.
Date Received
October 5, 1987
Decision Date
December 14, 1987
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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Other Clearances by Interpro Intl., Inc.

K Number Device Name
K890968 VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)
K890891 LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)
K891642 PATIENT EXAMINATION GLOVES (LATEX)
K891438 PATIENT EXAMINATION GLOVES (LATEX)
K891440 PATIENT EXAMINATION GLOVES (LATEX)
K881374 SURGEONS GLOVES
K874766 INTERPRO INT'L, INC. ISOLATION GOWN
K874066 SURGICAL CAPS
K874064 SHOE COVERS
K874065 LAPAROTOMY SPONGES
Search all 11 clearances from Interpro Intl., Inc. →