ADVANCED HAND HELD CO2 LASER/HH-550 FOR DGGD USE— 510(k) K864948

Name: FDA 510(k) clearance K864948
Creator: U.S. Food and Drug Administration
Published: 1987-03-30

Substantially Equivalent

Bio Quantum Technologies, Inc.

FDA 510(k) clearance K864948 for ADVANCED HAND HELD CO2 LASER/HH-550 FOR DGGD USE, Substantially Equivalent on 1987-03-30. Applicant: Bio Quantum Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Bio Quantum Technologies, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1986-12-17
Decision date: 1987-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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K934089 — BIO QUANTUM TECHNOLOGIES, INC. HAND-HELD CO2 LASER SYSTEM MODEL HH-550S1994-02-03
K864946 — ADVANCED HAND HELD CO2 LASER/HH-550 FOR DOED USE1988-01-28
K864887 — ADVANCED HAND HELD CO2 LASER MODEL HH-550 FOR SU1987-04-10
K840406 — MICROSURGICAL CO2 LASER SYS - 41001984-08-20
K837110 — MODEL 4100 MICROSURGICAL CO2 LASER SYSTEM1983-03-11

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