HOTIP HEMOSTATIC PROBE— 510(k) K843628

Substantially Equivalent

Trimedyne, Inc.

FDA 510(k) clearance K843628 for HOTIP HEMOSTATIC PROBE, Substantially Equivalent on 1985-11-12. Applicant: Trimedyne, Inc.. Device class: 2.

Clearance details

Applicant: Trimedyne, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1984-09-14
Decision date: 1985-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LNK

K925395 — TECHNOMED PULSOLITH 4000 LASER SYSTEM1993-05-21
K901723 — MDL-2000 LASERTRIPTER1990-07-13
K874253 — ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.1988-07-12
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

More clearances from Trimedyne, Inc.

K053457 — VAPORMAX II2005-12-21
K050412 — VAPORMAX2005-03-14
K043012 — OMNIPULSE MINI, MODEL 21202004-11-17
K041660 — TRIMEDYNE HOLMIUM LASER SYSTEMS2004-09-08
K022655 — TRIMEDYNE SIDE FIRING NEEDLE WITH VENT SHEATH2002-11-07

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