510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770765Substantially Equivalent

Reagent Set, Renorpace

G.D. Searle and Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770765 is the FDA 510(k) clearance record for REAGENT SET, RENORPACE, a class I device, cleared for G.D. Searle and Co. on under FDA product code DPA (Apparatus, General Use, Thin Layer Chromatography). FDA records list 56 510(k) clearances for G.D. Searle and Co., from to . As of , FDA records show no recalls naming K770765.

Clearance record

Decision date
Received
(58 days to decision)
Product code
DPA Apparatus, General Use, Thin Layer Chromatography
Regulation
21 CFR 862.2270
Device class
Class I
Review panel
Clinical Chemistry
Applicant
G.D. Searle and Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DPA

Trailing 12 months

FDA records hold no clearances under product code DPA in the trailing twelve months.

FDA records show no clearances under product code DPA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DPA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260