510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122379Substantially Equivalent

Flash Pta Balloon Dilatation Catheter - 4Mm X 14Mm X 135Cm, Flash Pta Balloon Dilatation Catheter - 4Mm X 19Mm X 135Cm

Verge Medical Inc., Mountain View CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122379 is the FDA 510(k) clearance record for FLASH PTA BALLOON DILATATION CATHETER - 4MM X 14MM X 135CM, FLASH PTA BALLOON DILATATION CATHETER - 4MM X 19MM X 135CM, a class II device, cleared for Ostial Corporation on under FDA product code LIT (Catheter, Angioplasty, Peripheral, Transluminal). FDA records list 14 510(k) clearances for Verge Medical Inc., from to . As of , FDA records show one recall naming K122379.

Clearance record

Decision date
Received
(30 days to decision)
Product code
LIT Catheter, Angioplasty, Peripheral, Transluminal
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Ostial Corporation 510 Clyde Ave., Mountain View CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LIT

Trailing 12 months
5 clearances under product code LIT in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LIT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20262
October 20260