MDL-2000 LASERTRIPTER— 510(k) K901723

Substantially Equivalent

Candela Laser Corp.

FDA 510(k) clearance K901723 for MDL-2000 LASERTRIPTER, Substantially Equivalent on 1990-07-13. Applicant: Candela Laser Corp.. Device class: 2.

Clearance details

Applicant: Candela Laser Corp.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1990-04-16
Decision date: 1990-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayland, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LNK

K925395 — TECHNOMED PULSOLITH 4000 LASER SYSTEM1993-05-21
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K874255 — ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.1988-07-12
K880193 — MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USE1988-04-14
K880256 — MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USE1988-04-14

More clearances from Candela Laser Corp.

K951033 — ANDELA DYNAMIC COOLING DEVICE1996-08-15
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K955011 — CANDELA HCS 2000 URETHERAL WARMER CATHETER1996-04-03
K954872 — CANDELA CRYO-PROBE HOLDER1996-02-05
K954934 — CANDELA SPTL LONG PULSE/TUNABLE PULSED DYE LASE1996-02-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.