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

PHARMANET (TM)

K Number: K872572 · Decision Jan 14, 1988
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
129
Review Days
199

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Basic Information

Device Name
PHARMANET (TM)
K Number
K872572
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Pharmacia, Inc.
Date Received
June 29, 1987
Decision Date
January 14, 1988
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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