PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.— 510(k) K875007

Name: FDA 510(k) clearance K875007
Creator: U.S. Food and Drug Administration
Published: 1988-03-14

Substantially Equivalent

Advanced Surgical Products, Inc.

FDA 510(k) clearance K875007 for PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA., Substantially Equivalent on 1988-03-14. Applicant: Advanced Surgical Products, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Surgical Products, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1987-12-04
Decision date: 1988-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterfield, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FST

view all

K200874 — TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End2020-06-30
K141330 — ENDO-CORD2014-12-15
K122637 — LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 480899992012-11-01
K113697 — EIGR SURGICAL ILLUMINATION SYSTEM2012-02-10
K113330 — CABLECAP2012-01-12

More clearances from Advanced Surgical Products, Inc.

view all

K030926 — FAST THROW STAINLESS STEEL SURGICAL SUTURE2003-07-21
K895800 — ADVANCED SURGICAL SOLID STATE BIPOLAR COAGULATOR1990-01-22
K896754 — I/A HANDPIECE1990-01-11
K896305 — MULTI-USE I/A HANDPIECE1989-12-18
K884557 — ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE1989-05-12

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