510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913129Substantially Equivalent

Angiolaz Angioscope Catheter

Angiolaz, Inc., Rockingham VT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913129 is the FDA 510(k) clearance record for ANGIOLAZ ANGIOSCOPE CATHETER, a class II device, cleared for Angiolaz, Inc. on under FDA product code LYK (Angioscope). FDA records list 10 510(k) clearances for Angiolaz, Inc., from to . As of , FDA records show no recalls naming K913129.

Clearance record

Decision date
Received
(164 days to decision)
Product code
LYK Angioscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Angiolaz, Inc. Rte. 103 Transportation Park, Rockingham VT
510(k) summary
Statement
Third party review
No

Clearances, product code LYK

Trailing 12 months
1 clearance under product code LYK in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LYK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260