510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K211572Substantially Equivalent

Aesculap Slim Clip Applier

Aesculap Inc, Center Valley PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211572 is the FDA 510(k) clearance record for Aesculap Slim Clip Applier, a class II device, cleared for Aesculap, Inc. on under FDA product code HCI (Applier, Aneurysm Clip). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K211572.

Clearance record

Decision date
Received
(206 days to decision)
Product code
HCI Applier, Aneurysm Clip
Regulation
21 CFR 882.4175
Device class
Class II
Review panel
Neurology
Applicant
Aesculap, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HCI

Trailing 12 months

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

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