Reliant Technologies, Inc.
Reliant Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2008.
Top product codes for Reliant Technologies, Inc.
Recent clearances by Reliant Technologies, Inc.
- K080915 — FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIES
- K071051 — FRAXEL III SR LASER SYSTEM AND ACCESSORIES
- K071621 — RELIANT TECHNOLOGIES C300 CHILLER SYSTEM AND ACCESSORIES
- K070284 — FRALEX SR 1500 LASER SYSTEM (FRALEX II SR LASER SYSTEM)
- K063038 — FRAXEL III SR LASER SYSTEM AND ACCESSORIES
- K063808 — FRAXEL IV SR LASER SYSTEM
- K062303 — FRAXEL II SR LASER SYSTEM
- K060310 — FRAXEL II SR LASER SYSTEM AND ACCESSORIES
- K053047 — FRAXEL SR LASER SYSTEM
- K050841 — FRAXEL SR LASER SYSTEM
- K042319 — RELIANT LASER II SYSTEM AND ACCESSORIES
- K040617 — RELIANT LASER SYSTEM II
- K031795 — RELIANT LASER SYSTEM
- K023050 — RELIANT BTL 5000 PULS ELECTRICAL STIMULATION SYSTEM, RELIANT BTL 5000 SONO ULTRASOUND SYSTEM, RELIANT BTL 5000 COMBI
- K971821 — UNICA 315 M CO2 SURGICAL LASER SYSTEM
- K953670 — ACCUSCAN MODEL C CO2 LASER SCANNER
- K944437 — DISPOSABLE LASER SWEEP TIP
- K942935 — ACUTOME 100 COLOR-CORRECTED CO2 LASER HANDPIECE
- K943045 — UNIMAX MODEL 2500 MULTIWAVELENGTH COLOR CORRECTED
Data sourced from openFDA. This site is unofficial and independent of the FDA.