FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FE-CULT PLUS

K Number: K820072 · Decision Mar 4, 1982
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
96
Applicant Total
21
Review Days
51

Basic Information

Device Name
FE-CULT PLUS
K Number
K820072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
GAMMA BIOLOGICALS, INC.
Date Received
January 12, 1982
Decision Date
March 4, 1982
Product Code
KHE
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KHE Reagent, Occult Blood

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Other Clearances by GAMMA BIOLOGICALS, INC.

K Number Device Name
K864207 DISPOSABLE TEST CARDS/GAMMA SLIDE TEST INFECT MONO
K861016 GAMMA SLIDE TEST FOR INFECTIOUS MONONUCLEOSIS
K832473 GAMMA SLIDE TEST FOR PREGNANCY
K820647 GAMMA FETAL BLEED SCREENING TEST
K813342 GAMMA CHLOROQUINE DIPHOSPHATE SOLUTION
K811752 FE-CULT PLUS
K802534 GAMMA PI BLOOD GROUP SUBSTANCE
K802533 GAMMA LEWIS BLOOD GROUP SUBSTANCE
K800658 RST-SERIES CONTROL
K792582 POLY-LEC SYSTEM
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