510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K934378Substantially Equivalent

Scimed Maverick Percutaneous Transluminal Angioplasty (Pta) Catheter

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

K934378 is the FDA 510(k) clearance record for SCIMED MAVERICK PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, a class II device, cleared for Scimed Life Systems, Inc. on under FDA product code LIT (Catheter, Angioplasty, Peripheral, Transluminal). FDA records list 109 510(k) clearances for Scimed Life Systems, Inc., from to . As of , FDA records show no recalls naming K934378.

Clearance record

Decision date
Received
(131 days to decision)
Product code
LIT Catheter, Angioplasty, Peripheral, Transluminal
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Scimed Life Systems, Inc. 2905 Northwest Blvd., Plymouth MN
510(k) summary
Summary
Third party review
No

Clearances, product code LIT

Trailing 12 months
5 clearances under product code LIT in the twelve months to November 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LIT, trailing twelve months
MonthClearances
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20262
October 20260
November 20260