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

DIGOXIN STANDARDS IN HUMAN SERUM

K Number: K780889 · Decision Aug 14, 1978
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
29
Review Days
75

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Basic Information

Device Name
DIGOXIN STANDARDS IN HUMAN SERUM
K Number
K780889
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Pcl-Ria, Inc.
Date Received
May 31, 1978
Decision Date
August 14, 1978
Product Code
DMP
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DMP Digoxin Control Serum, Ria

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Other Clearances by Pcl-Ria, Inc.

K Number Device Name
K830526 B-GCG SYSTEM BY RIA
K822935 THYROID STIMULATING HORMONE
K823014 DIGOXIN KIT
K822612 T3 UPTAKE KITS
K820886 THYROXINE T4 KIT
K820358 FOLLICLE STIMULATING HORMONE KIT
K820357 LUTEINIZING HORMONE KIT
K812666 THYROXINE (T4) 125I
K810867 FOLLICLE STIMULATING HORMONE (FSH)
K810852 FOLLICLE STIMULATING HORMONE ANTISERUM
Search all 29 clearances from Pcl-Ria, Inc. →