FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

ASO SLIDE TEST

K Number: K881209 · Decision Apr 12, 1988
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
36
Applicant Total
15
Review Days
22

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Basic Information

Device Name
ASO SLIDE TEST
K Number
K881209
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Ncs Diagnostics, Inc.
Date Received
March 21, 1988
Decision Date
April 12, 1988
Product Code
GTQ
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
GTQ Antistreptolysin - Titer/Streptolysin O Reagent

Similar 510(k) Clearances

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

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Other Clearances by Ncs Diagnostics, Inc.

K Number Device Name
K943498 KULTSURE STARSWAB (M210), MODIFICATION
K943499 KULTSURE STARSWAB(M240), MODIFICATION
K882811 STREPSLIDE
K874019 STAPHSLIDE
K871404 KULTSURE
K870231 KULTSURE
K860178 KULTSURE (CULTURE TRANSPORT)
K860655 KULTSURE (CATALOGUE NO. M200)
K860657 KULTSURE (CATALOGUE NO. M240)
K860656 KULTSURE (CATALOGUE NO. M210)
Search all 15 clearances from Ncs Diagnostics, Inc. →