FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GLYCOSYLATED HEMOGLOBIN KIT

K Number: K801561 · Decision Aug 12, 1980
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
94
Review Days
35

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
GLYCOSYLATED HEMOGLOBIN KIT
K Number
K801561
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
July 8, 1980
Decision Date
August 12, 1980
Product Code
LCP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
LCP Assay, Glycosylated Hemoglobin

Similar 510(k) Clearances

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

View all

Other Clearances by Amersham Corp.

K Number Device Name
K914135 AMERLITE(TM) PROLACTIN-30 ASSAY, LAN.0086/2086
K912733 AMERLEX-M SPECIFIC ESTROL(UNCONJUGATED) RIA KIT
K912766 AMERLITE CK-MB ASSAY
K904666 AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008
K902760 AMERSHAM TSH CONTROL SERA
K901854 GADOLINIUM-153 BONE DENSITOMETER (GDC.10411/10412)
K901857 GADOLINIUM-153 BONE DENSITOMETER (GDC.10413)
K901848 GADOLINIUM-153 BONE DENSITOMETER SOURCES
K901832 GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415
K896270 AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
Search all 94 clearances from Amersham Corp. →