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

BIOTIS ACETAMIDE AGAR

K Number: K862389 · Decision Jul 3, 1986
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
284
Applicant Total
98
Review Days
9

Basic Information

Device Name
BIOTIS ACETAMIDE AGAR
K Number
K862389
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2360
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
OTISVILLE BIOTECH, INC.
Date Received
June 24, 1986
Decision Date
July 3, 1986
Product Code
JSI
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
JSI Culture Media, Selective And Differential

Similar 510(k) Clearances

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Other Clearances by OTISVILLE BIOTECH, INC.

K Number Device Name
K862387 BIOTIS HAEMOPHILUS IDENTIFICATION QUAD
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
K862392 BIOTIS MOTILITY TEST MEDIUM
Search all 98 clearances from OTISVILLE BIOTECH, INC. →