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

AMES DCA 2000 HEMOGLOBIN ALC CONTROLS

K Number: K940971 · Decision Jul 19, 1994
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
145
Review Days
139

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
AMES DCA 2000 HEMOGLOBIN ALC CONTROLS
K Number
K940971
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
March 2, 1994
Decision Date
July 19, 1994
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 Heraeus Kulzer, Inc.

K Number Device Name
K091494 FLEXITIME FLOW
K063062 HKBOND 2006
K060994 MONDIAL
K052543 HERACERAM ZIRKONIA
K043504 PALAIMPACT
K043295 VERSYO.DIRECT
K042878 FLEXITIME XTREME
K030052 OSTIM
K040859 HERACERAM PRESS
K040043 NDX-40 ALLOY
Search all 145 clearances from Heraeus Kulzer, Inc. →