Atlas FDA

CHOCOLATE AGAR

FDA 510(k) clearance K841749 · decided 1984-05-31

Clearance details

K-number
K841749
Device name
CHOCOLATE AGAR
Applicant
The Montana Deaconess Medical Center
Decision
Substantially Equivalent
Date received
1984-04-27
Decision date
1984-05-31
Days to decision
34 days
Clearance type
Traditional
Product code
KZI
Device class
1
Regulation number
866.2330
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
LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) (K884208)Oxoid U.S.A., Inc.1988-10-25
DIAMOND'S MEDIUM MODIFIED (K881995)Remel Co.1988-06-02
MIDDLEBROOK 7H9 BROTH (K880122)Hardy Media1988-03-31
MIDDLEBROOK 7H11 AGAR (K880134)Hardy Media1988-03-31
LOWENSTEIN-JENSEN, GRUFT (K880131)Hardy Media1988-03-31
WALLENSTEIN MEDIUM SLANT (K880138)Hardy Media1988-03-30
CYSTINE TRYPTIC MEDIUM BASE (K880109)Hardy Media1988-03-30
POTATO DEXTROSE AGAR (K880127)Hardy Media1988-03-07
BIOTIS (TM) SABHI (DOUBLE POUR) (K874179)Otisville Biopharm, Inc.1988-01-28
BIOTIS (TM) BCYE (K874177)Otisville Biopharm, Inc.1987-12-04
ECG BASED MEDIA (K873267)Central Media1987-11-04
MIDDLEBROOK BASED MEDIA (K873266)Central Media1987-10-28

Recalls involving this device

No recalls on record reference this clearance.