510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K992053Substantially Equivalent

Aesculap Vascular Instruments

Aesculap Inc, South San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992053 is the FDA 510(k) clearance record for AESCULAP VASCULAR INSTRUMENTS, a class II device, cleared for Aesculap, Inc. on under FDA product code DXC (Clamp, Vascular). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K992053.

Clearance record

Decision date
Received
(209 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
Aesculap, Inc. 1000 Gateway Blvd., South San Francisco CA
510(k) summary
Summary
Third party review
No

Clearances, product code DXC

Trailing 12 months
5 clearances under product code DXC in the twelve months to November 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXC, trailing twelve months
MonthClearances
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20261
August 20260
September 20260
October 20260
November 20260