Atlas FDA

BLASTOMYCES DERMATITIDIS, ANTISERUM

FDA 510(k) clearance K792685 · decided 1980-01-17

Clearance details

K-number
K792685
Device name
BLASTOMYCES DERMATITIDIS, ANTISERUM
Applicant
Meridian Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1979-12-27
Decision date
1980-01-17
Days to decision
21 days
Clearance type
Traditional
Product code
KFH
Device class
2
Regulation number
866.3060
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
EXO-ANTIGEN IDENTIFICATION SYSTEM CAT.# EX1001 (K880029)Immuno-Mycologics, Inc.1988-02-24
BLASTOMYCES DERMATITIDIS POS/CONTROL (K792681)Meridian Diagnostics, Inc.1980-01-17
ANTI-BLASTOMYCES CONTROL SERUM (YEAST) (K760833)I M, Inc.1976-11-01

Recalls involving this device

No recalls on record reference this clearance.