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

MOTILITY INDOLE ORNITHINE AGAR

K Number: K850547 · Decision Mar 11, 1985
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
52
Applicant Total
114
Review Days
28

Basic Information

Device Name
MOTILITY INDOLE ORNITHINE AGAR
K Number
K850547
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
HARDY MEDIA
Date Received
February 11, 1985
Decision Date
March 11, 1985
Product Code
JSE
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
JSE Culture Media, Multiple Biochemical Test

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Other Clearances by HARDY MEDIA

K Number Device Name
K880126 LAURYL TRYPTOSE BROTH
K880122 MIDDLEBROOK 7H9 BROTH
K880131 LOWENSTEIN-JENSEN, GRUFT
K880124 LOWENSTEIN-JENSEN, W/NACL
K880120 MOELLERS DECARBOXYLASE, LYSINE
K880125 LOWENSTEIN-JENSEN, SELECTIVE
K880119 MOELLERS DECARBOXYLASE, ONITHINE
K880116 MRVP BROTH
K880121 MOELLERS DECARBOXYLASE, BASE
K880134 MIDDLEBROOK 7H11 AGAR
Search all 114 clearances from HARDY MEDIA →