FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

VDRL CARBON ANTIGEN TEST S900500, S900250 & S90010

K Number: K851504 · Decision Aug 19, 1985
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
8
Applicant Total
15
Review Days
126

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Basic Information

Device Name
VDRL CARBON ANTIGEN TEST S900500, S900250 & S90010
K Number
K851504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3820
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Ncs Diagnostics, Inc.
Date Received
April 15, 1985
Decision Date
August 19, 1985
Product Code
GMP
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
GMP Antisera, Control For Nontreponemal Tests

Similar 510(k) Clearances

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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
K881209 ASO SLIDE TEST
K874019 STAPHSLIDE
K871404 KULTSURE
K870231 KULTSURE
K860178 KULTSURE (CULTURE TRANSPORT)
K860655 KULTSURE (CATALOGUE NO. M200)
K860657 KULTSURE (CATALOGUE NO. M240)
Search all 15 clearances from Ncs Diagnostics, Inc. →