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

ASSAYED CHOLINESTERASE CONTROL

K Number: K885282 · Decision Jun 9, 1989
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
4
Review Days
171

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Basic Information

Device Name
ASSAYED CHOLINESTERASE CONTROL
K Number
K885282
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Actio, Inc.
Date Received
December 20, 1988
Decision Date
June 9, 1989
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

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Other Clearances by Actio, Inc.

K Number Device Name
K902699 SHAPE-ACTIO URINALYSIS CONTROLS(ASSAYED & UNASSAY)
K890721 SHAPE-ACTIO METAL TOXICOLOGY CONTROL
K890442 SHAPE-ACTIO URINALYSIS CONTROLS