SURGILASE YAG 100 FOR GYNECOLOGY USE— 510(k) K881499

Name: FDA 510(k) clearance K881499
Creator: U.S. Food and Drug Administration
Published: 1988-04-29

Substantially Equivalent

Surgilase, Inc.

FDA 510(k) clearance K881499 for SURGILASE YAG 100 FOR GYNECOLOGY USE, Substantially Equivalent on 1988-04-29. Applicant: Surgilase, Inc.. Device class: 2.

Clearance details

Applicant: Surgilase, Inc.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1988-03-22
Decision date: 1988-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warwick, RI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLO

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K884815 — SLT CLMD CONTACT LASER1988-12-22
K880592 — LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE1988-04-25
K880170 — MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS1988-03-24
K874254 — ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS1988-03-04
K875104 — SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE1988-02-02

More clearances from Surgilase, Inc.

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K932421 — SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASE1993-10-15
K924664 — SURGILASE FIBERLASE CO2 LASER WAVEGUIDE1993-04-15
K905006 — SURGILASE SL 150 SURGICAL LASER SYSTEM1991-02-21
K904203 — SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEM1990-12-07
K902211 — SURGILASE YAG 100 SURGICAL LASER SYSTEM1990-06-29

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