Atlas FDA

RAPID FERMENTATION AGAR (RFA)

FDA 510(k) clearance K800734 · decided 1980-05-08

Clearance details

K-number
K800734
Device name
RAPID FERMENTATION AGAR (RFA)
Applicant
Remel Co.
Decision
Substantially Equivalent
Date received
1980-04-02
Decision date
1980-05-08
Days to decision
36 days
Clearance type
Traditional
Product code
JSE
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
MLX MICROTITER PLATE LUMINOMETER (K962265)Dynatech Laboratories, Inc.1996-07-25
X-ACT LDC/IND (K883996)Pro-Lab, Inc.1988-10-12
X-ACT UREA/TDA (K883995)Pro-Lab, Inc.1988-10-12
MRVP BROTH (K880116)Hardy Media1988-03-31
MIL MEDIUM (K880133)Hardy Media1988-03-31
KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGAR (K874537)Lakewood Biochemical Co., Inc.1987-11-20
CYSTINE TRYPTIC AGAR W/O CARBOHYDRATES (K871096)bioMerieux, Inc.1987-04-03
MICRODILUTION IDENTIFICATION PANELS (K864674)American Micro Scan1987-01-05
BIOTIS LITMUS MILK (K862393)Otisville Biotech, Inc.1986-07-03
BIOTIS TSI (K860413)Otisville Biotech, Inc.1986-02-24
BIOTIS ORNITHINE INDOLE MOTILITY MEDIA (K860414)Otisville Biotech, Inc.1986-02-24
BIOTIS SIM MEDIUM (K860412)Otisville Biotech, Inc.1986-02-24

Recalls involving this device

No recalls on record reference this clearance.