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

ANTI-HUMAN LAMBDA SERUM

K Number: K791283 · Decision Nov 27, 1979
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
52
Applicant Total
12
Review Days
140

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Basic Information

Device Name
ANTI-HUMAN LAMBDA SERUM
K Number
K791283
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Diagnostica, Inc.
Date Received
July 10, 1979
Decision Date
November 27, 1979
Product Code
DEH
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DEH Lambda, Antigen, Antiserum, Control

Similar 510(k) Clearances

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Other Clearances by Diagnostica, Inc.

K Number Device Name
K002756 EASE-A-CULT
K823348 H. INFLUENZA B ANTISERA FOR CIE
K812434 DIAGNOSTIC KITS & KIT COMPONENTS
K800398 PARACONTROL ABNORMAL IMMUNOGLOBULIN CONT
K791281 ANTI-HUMAN IGG SERUM
K791284 ANTI-HUMAN KAPPA SERUM
K791285 ANTI-HUMAN GLOBULINS
K791282 ANTI-HUMAN SERUM
K790672 ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU
K790671 DERMATOPHYTIN O
Search all 12 clearances from Diagnostica, Inc. →