510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864948Substantially Equivalent

Advanced Hand Held CO2 Laser/hh-550 for Dggd Use

Bio Quantum Technologies, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864948 is the FDA 510(k) clearance record for ADVANCED HAND HELD CO2 LASER/HH-550 FOR DGGD USE, a class II device, cleared for Bio Quantum Technologies, Inc. on under FDA product code LNK (Laser For Gastro-Urology Use). FDA records list 6 510(k) clearances for Bio Quantum Technologies, Inc., from to . As of , FDA records show no recalls naming K864948.

Clearance record

Decision date
Received
(103 days to decision)
Product code
LNK Laser For Gastro-Urology Use
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Bio Quantum Technologies, Inc. 8275 El Rio, Suite 180, Houston TX
Third party review
No

Clearances, product code LNK

Trailing 12 months

FDA records hold no clearances under product code LNK in the trailing twelve months.

FDA records show no clearances under product code LNK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LNK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260