Gamma Biologicals, Inc.
Gamma Biologicals, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1986.
Top product codes for Gamma Biologicals, Inc.
Recent clearances by Gamma Biologicals, Inc.
- 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
- K820072 — FE-CULT PLUS
- K811752 — FE-CULT PLUS
- K802533 — GAMMA LEWIS BLOOD GROUP SUBSTANCE
- K802534 — GAMMA PI BLOOD GROUP SUBSTANCE
- K800658 — RST-SERIES CONTROL
- K792582 — POLY-LEC SYSTEM
- K792583 — GAMMA ARACHIS HYPOGEA LECTIN
- K790973 — LO-ION
- K760034 — TEST, STREP, LATEX SLIDE
- K760032 — TEST, MONO., DIFFERENTIAL SLIDE
- K760033 — TEST, ANTIBODIES FOR GRP A, LATEX SLIDE
- K760035 — TEST, C-REATIVE PROTEIN, LATEX SLIDE
- K760036 — TEST, LATEX SLIDE, RHEUMATOID FACTOR
- K760096 — REAGENT, LYOPHILIZED ANTI-STREPTOLYSIN O
- K760097 — FEBRILE ANTIGENS & CONTROL SERUMS
- K760098 — REAGENT, VDRL
Data sourced from openFDA. This site is unofficial and independent of the FDA.