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

BIO INTERFERENCE BLANKING MATERIAL

K Number: K823687 · Decision Jan 7, 1983
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
73
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIO INTERFERENCE BLANKING MATERIAL
K Number
K823687
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Monitor Corp.
Date Received
December 7, 1982
Decision Date
January 7, 1983
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.

View all

Other Clearances by American Monitor Corp.

K Number Device Name
K895999 PHOSPHORUS
K896000 ASPARTATE AMINOTRANFERASE (AST)
K896001 ALANINE AMINOTRANSFERASE (ALT)
K895423 ACCESS CHEMISTRY ANALYZER
K893137 EXCEL (TM) CHEMISTRY ANALYZER
K892331 ENZYMATIC UREA NITROGEN REAGENT SET
K893479 CHOLESTEROL REAGENT SET
K892002 NEOCHROME(R) III GLUCOSE
K890312 GAMMA-GLUTAMYLTRANSFERASE
K890034 PHOTOMETRIC METHOD, IRON (NON-HEME) (75JIY)
Search all 73 clearances from American Monitor Corp. →