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

DERMATOPHYTIN O

K Number: K790671 · Decision May 31, 1979
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
15
Applicant Total
12
Review Days
55

Basic Information

Device Name
DERMATOPHYTIN O
K Number
K790671
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
DIAGNOSTICA, INC.
Date Received
April 6, 1979
Decision Date
May 31, 1979
Product Code
JXB
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
JXB Kit, Identification, Yeast

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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
K791283 ANTI-HUMAN LAMBDA SERUM
K791284 ANTI-HUMAN KAPPA SERUM
K791281 ANTI-HUMAN IGG SERUM
K791282 ANTI-HUMAN SERUM
K791285 ANTI-HUMAN GLOBULINS
K790672 ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU
Search all 12 clearances from DIAGNOSTICA, INC. →