Atlas FDA

MACCONKEY AGAR (PLATE)

FDA 510(k) clearance K791556 · decided 1979-09-17

Clearance details

K-number
K791556
Device name
MACCONKEY AGAR (PLATE)
Applicant
American Laboratory Supply, Inc.
Decision
Substantially Equivalent
Date received
1979-08-17
Decision date
1979-09-17
Days to decision
31 days
Clearance type
Traditional
Product code
JSH
Device class
1
Regulation number
866.2320
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
DNASE TEST AGAR (K881486)Acumedia Manufacturers, Inc.1988-04-18
UREA AGAR BASE (K881559)Acumedia Manufacturers, Inc.1988-04-18
RUSSELL DOUBLE SUGAR AGAR (K881553)Acumedia Manufacturers, Inc.1988-04-18
UREA BROTH (K881560)Acumedia Manufacturers, Inc.1988-04-18
PHENOL RED BROTH BASE (K881551)Acumedia Manufacturers, Inc.1988-04-18
FLO AGAR (K881540)Acumedia Manufacturers, Inc.1988-04-18
MOELLERS DECARBOXYLASE, BASE (K880121)Hardy Media1988-03-31
OF MEDIUM BASE (K880117)Hardy Media1988-03-30
ACTINOMYCETE DIFFERENTIAL MEDIA (K873270)Central Media1987-11-04
MAINTENANCE & CARBOHYDRATE FERMENTATION MEDIA (K873263)Central Media1987-10-28
SIMMONS CITRATE MEDIUM SLANT, PRODUCT #T3084 (K873411)Lakewood Biochemical Co., Inc.1987-10-06
MOTILITY INDOLE ORNATHINE (MIO) PRODUCT #T3053 (K873704)Lakewood Biochemical Co., Inc.1987-10-02

Recalls involving this device

No recalls on record reference this clearance.