510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K894669Substantially Equivalent

Laser Shielding Tube

Vitaid, Ltd., M5m 2e1, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894669 is the FDA 510(k) clearance record for LASER SHIELDING TUBE, a class II device, cleared for Vitaid, Ltd. on under FDA product code BTR (Tube, Tracheal (W/Wo Connector)). FDA records list 7 510(k) clearances for Vitaid, Ltd., from to . As of , FDA records show no recalls naming K894669.

Clearance record

Decision date
Received
(81 days to decision)
Product code
BTR Tube, Tracheal (W/Wo Connector)
Regulation
21 CFR 868.5730
Device class
Class II
Review panel
Anesthesiology
Applicant
Vitaid, Ltd. 147 Old Orchard Grove, M5m 2e1, CA
Third party review
No

Clearances, product code BTR

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