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

BIOTIS ORNITHINE INDOLE MOTILITY MEDIA

K Number: K860414 · Decision Feb 24, 1986
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
52
Applicant Total
98
Review Days
21

Basic Information

Device Name
BIOTIS ORNITHINE INDOLE MOTILITY MEDIA
K Number
K860414
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
OTISVILLE BIOTECH, INC.
Date Received
February 3, 1986
Decision Date
February 24, 1986
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JSE), ordered by most recent decision date.

View all

Other Clearances by OTISVILLE BIOTECH, INC.

K Number Device Name
K862387 BIOTIS HAEMOPHILUS IDENTIFICATION QUAD
K862389 BIOTIS ACETAMIDE AGAR
K862398 BIOTIS DECARBOXYLASE MEDIA, ORNITHINE
K862400 BIOTIS KV LAKED BLOOD AGAR
K862391 BIOTIS DESOXYCHOLATE AGAR
K862395 BIOTIS DECARBOXYLASE MEDIA, BASE
K862393 BIOTIS LITMUS MILK
K862388 BIOTIS TCBS AGAR
K862397 BIOTIS DECARBOXYLASE MEDIA, LYSINE
K862396 BIOTIS DECARBOXYLASE MEDIA, ARGININE
Search all 98 clearances from OTISVILLE BIOTECH, INC. →