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

REAGENT SET, RENORPACE

K Number: K770765 · Decision Jun 24, 1977
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
4
Applicant Total
56
Review Days
58

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Basic Information

Device Name
REAGENT SET, RENORPACE
K Number
K770765
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2270
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
G.D. Searle and Co.
Date Received
April 27, 1977
Decision Date
June 24, 1977
Product Code
DPA
Advisory Committee
Clinical Chemistry
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
DPA Apparatus, General Use, Thin Layer Chromatography

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K Number Device Name
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K811071 VENOUS OXYGEN PROBE
K803238 INTRAVASCULAR CATHETER
K810630 SILICONE ELASTOMER COATED LATEX FOLEY
K810131 ADMINISTRATION SET
K802485 SEARLE VASCULAR LOOPS
K801805 METRONIDAZOLE DISCS
K810112 SWR DISPOSABLE PREP RAZOR
K802213 WHITE KNIGHT BOVIE CORD/SUCTION TUBE
Search all 56 clearances from G.D. Searle and Co. →