510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011487Substantially Equivalent

Correstore Patch, Models 1.5P2, 2P3, 3P4; Correstore Sizer, Model Crps

Somanetics Corp., Troy MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011487 is the FDA 510(k) clearance record for CORRESTORE PATCH, MODELS 1.5P2, 2P3, 3P4; CORRESTORE SIZER, MODEL CRPS, a class II device, cleared for Somanetics Corp. on under FDA product code DXZ (Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene). FDA records list 12 510(k) clearances for Somanetics Corp., from to . As of , FDA records show no recalls naming K011487.

Clearance record

Decision date
Received
(190 days to decision)
Product code
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Regulation
21 CFR 870.3470
Device class
Class II
Review panel
Cardiovascular
Applicant
Somanetics Corp. 1653 E. Maple Rd., Troy MI
510(k) summary
Summary
Third party review
No

Clearances, product code DXZ

Trailing 12 months

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

FDA records show no clearances under product code DXZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DXZ, 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