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

CDL ISOTONIC DILUENT

K Number: K822501 · Decision Sep 17, 1982
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
37
Applicant Total
14
Review Days
30

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
CDL ISOTONIC DILUENT
K Number
K822501
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.8200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Connecticut Diagnostics, Ltd.
Date Received
August 18, 1982
Decision Date
September 17, 1982
Product Code
GIF
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
GIF Diluent, Blood Cell

Similar 510(k) Clearances

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

View all

Other Clearances by Connecticut Diagnostics, Ltd.

K Number Device Name
K905617 VISI-STAPH
K822500 CDL LYSING REAGENT
K822504 CDL AUTO-LYSING REAGENT
K811222 INORGANIC PHOSPHORUS REAGENTS
K801898 URIC ACID DIAGNOSTIC REAGENT
K801897 GLUCOSE DIAGNOSTIC REAGENT
K792465 CONNECTICUT DIAGNOSTICS, LTS. DIRECT
K792338 DONNECT. DIAG. TOTAL BILIRUBIN REAGENTS
K792362 BLOOD UREA NITROGEN REAGENT
K792339 CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGEN
Search all 14 clearances from Connecticut Diagnostics, Ltd. →