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

LIQUI-SERA SERUM ALCOHOL CONTROLS

K Number: K881430 · Decision Jul 8, 1988
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
11
Review Days
94

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Basic Information

Device Name
LIQUI-SERA SERUM ALCOHOL CONTROLS
K Number
K881430
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biodiagnostic Intl
Date Received
April 5, 1988
Decision Date
July 8, 1988
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
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 Biodiagnostic Intl

K Number Device Name
K031296 LIQUI-HEME GLYCO A1C ASSAY
K874459 LIQUI-SERA SPINAL FLUID CONTROL
K863849 LIQUI-SERA COMBO LIGAND/TDM CONTROLS
K853906 LIQUI-SERA CHEMISTRY CONTROLS (COMPREHENSIVE)
K853887 LIQUI-SERA CHEM. MULTIPLE CALIBRATORS
K842668 LIQUI-HEME HEMOGLOBIN CALIBRATORS
K840618 LIQUI-URA CHEMISTRY URINE CONTROLS
K834398 LIQUI-SERA TDM CALIBRATORS
K834259 LIQUI-URA TOXIC URINE CONTROL
K831278 LIQUI-SERA ANTICONVULSANTS CONTROLS
Search all 11 clearances from Biodiagnostic Intl →