510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K935022Substantially Equivalent

Scimed Entre II Ptca Guide Wire Modification

Scimed Life Systems, Inc., Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935022 is the FDA 510(k) clearance record for SCIMED ENTRE II PTCA GUIDE WIRE MODIFICATION, a class II device, cleared for Scimed Life Systems, Inc. on under FDA product code DQX (Wire, Guide, Catheter). FDA records list 109 510(k) clearances for Scimed Life Systems, Inc., from to . As of , FDA records show no recalls naming K935022.

Clearance record

Decision date
Received
(90 days to decision)
Product code
DQX Wire, Guide, Catheter
Regulation
21 CFR 870.1330
Device class
Class II
Review panel
Cardiovascular
Applicant
Scimed Life Systems, Inc. 2010 E. Center Cir., Plymouth MN
510(k) summary
Summary
Third party review
No

Clearances, product code DQX

Trailing 12 months
12 clearances under product code DQX in the twelve months to November 2026, January 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQX, trailing twelve months
MonthClearances
December 20250
January 20263
February 20260
March 20263
April 20260
May 20261
June 20260
July 20262
August 20260
September 20262
October 20261
November 20260