Digoxin Clasp TM Ria Kit

FDA 510(k) K770069 · E. R. Squibb & Sons, Inc.

Substantially Equivalent

510(k) numberK770069

Submission

Device name
Digoxin Clasp TM Ria Kit
Applicant
E. R. Squibb & Sons, Inc.
New York, NY, US
Received
January 13, 1977
Decision date
January 18, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DPO – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3320
Specialty
Clinical Toxicology

Other 510(k)s with product code DPO

510(k)DeviceApplicantDecision
K914833Immulite DigoxinDPO · Traditional Cirrus Diagnostics, Inc.11/22/1991SE
K905719Eclipse Ica DigoxinDPO · Traditional Biotope, Inc.01/17/1991SE
K864449Digoxin/Ria Kit Coated Tube Radioimmunoassay KitDPO · Traditional Canadian Bioclinical, Ltd.02/02/1987SE
K833842Ria Coat DigoxinDPO · Traditional Immuno Assay Corp.01/17/1984SE
K832163Sopheia Digoxin Eia KitDPO · Traditional Diagnostic Products Corp.08/12/1983SE
K830962Immuchem Covalent-Coat Ria KitDPO · Traditional Immuchem Corp.05/04/1983SE
K811932Coat-A-Count Digoxin RiaDPO · Traditional Diagnostic Products Corp.07/23/1981SE
K811776Kallestad Quanticoat 125 DigoxinDPO · Traditional Kallestad Laboratories, Inc.07/10/1981SE
K800205Ria Phase DigoxinDPO · Traditional Boehringer Mannheim Corp.03/19/1980SE
K791325Autopak 12 Digoxin Test Delivery SystemDPO · Traditional Micromedic Systems08/16/1979SE

More from Micromedic Systems

510(k)DeviceDecision
K821494Ria Stat 16JJJ · Traditional 06/03/1982SE
K820616Angiotensis I-Squibb RadioimmunoassayCIB · Traditional 03/26/1982SE
K820341Cortisol-Squibb Radioimmunoassay KitCGR · Traditional 03/04/1982SE
K820340T3 Uptake-Squibb Diagnostic KitKHQ · Traditional 03/04/1982SE
K811240Sur-Fit Loop Ostomy O.R. SetEXB · Traditional 06/16/1981SE
K811239Sur-Fit Disposable Convex InsertEXB · Traditional 06/09/1981SE
K811160Sur-Fit Irrigation SleeveEXD · Traditional 06/02/1981SE
K811163Sur-Fit Disposable Fange CapEXB · Traditional 05/21/1981SE
K810966Diagoxin Squibb Radioimmunoassay KitDNL · Traditional 04/21/1981SE
K810211T3 Ria KitCDP · Traditional 02/10/1981SE

Questions and answers

When was Digoxin Clasp TM Ria Kit cleared by the FDA?

Digoxin Clasp TM Ria Kit (K770069) received a 510(k) decision of Substantially Equivalent on January 18, 1977, 5 days after the submission was received.

What is the product code of K770069?

The FDA product code is DPO – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep., a Class II (moderate risk) device regulated under 21 CFR 862.3320.