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

CDL AUTO-LYSING REAGENT

K Number: K822504 · Decision Sep 17, 1982
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
14
Review Days
29

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Basic Information

Device Name
CDL AUTO-LYSING REAGENT
K Number
K822504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.8540
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Connecticut Diagnostics, Ltd.
Date Received
August 19, 1982
Decision Date
September 17, 1982
Product Code
GGK
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
GGK Products, Red-Cell Lysing Products

Similar 510(k) Clearances

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

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Other Clearances by Connecticut Diagnostics, Ltd.

K Number Device Name
K905617 VISI-STAPH
K822500 CDL LYSING REAGENT
K822501 CDL ISOTONIC DILUENT
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. →