FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER

K Number: K875275 · Decision Jan 27, 1988
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
11
Applicant Total
9
Review Days
34

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Basic Information

Device Name
WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER
K Number
K875275
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2540
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Sterling Drug, Inc.
Date Received
December 24, 1987
Decision Date
January 27, 1988
Product Code
JTQ
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JTQ Bath, Incubators/Water, All

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K820023 CONAGRAF TM DURAPATITE CONES
K813257 ALVEOGRAF DURAPATITE(18-40 MESH)
K813070 PERIOGRAF
K780209 DILUTION SPIKE