510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811236Substantially Equivalent

Disposable Holder for Hancock Aortic

Vascor, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811236 is the FDA 510(k) clearance record for DISPOSABLE HOLDER FOR HANCOCK AORTIC, a class I device, cleared for Vascor, Inc. on under FDA product code DTJ (Holder, Heart-Valve, Prosthesis). FDA records list 2 510(k) clearances for Vascor, Inc. As of , FDA records show no recalls naming K811236.

Clearance record

Decision date
Received
(9 days to decision)
Product code
DTJ Holder, Heart-Valve, Prosthesis
Regulation
21 CFR 870.3935
Device class
Class I
Review panel
Cardiovascular
Applicant
Vascor, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DTJ

Trailing 12 months

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

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