ClearanceBrief
Company ยท US

Pfizer Pharmaceuticals

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1989. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FMINeedle, Hypodermic, Single Lumen1
FRODressing, Wound, Drug1
GMYAntisera, Fluorescent, All Types, Escherichia Coli1
JHXFluorometric Method, Cpk Or Isoenzymes1
JSCCulture Media, General Nutrient Broth1
JTNSusceptibility Test Discs, Antimicrobial1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 22, 1989K885321WATER JEL STERILE GEL-SOAKED BURN DRESSING
Pfizer Pharmaceuticals
FRO
Mar 31, 1981K810427CEFOTAXIME 30MCG ANTIMICROBIAL SUSCEP.
Pfizer Pharmaceuticals
JTN
Oct 23, 1980K802408E-VAC BLOOD CULTURE SYSTEM
Pfizer Pharmaceuticals
JSC
Sep 15, 1977K771605CREATINE KINASE ISOENZYME SUBSTRATE SET
Pfizer Pharmaceuticals
JHX
May 25, 1977K770801MICROBIO. PROD. FLUORESCENT ANTIBODY
Pfizer Pharmaceuticals
GMY
Apr 15, 1977K770425NEEDLES, STERILE, AIRWAY
Pfizer Pharmaceuticals
FMI

Latest recalls

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