HGM, INC. LASERCATH (STERILE)— 510(k) K860357

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K860357 for HGM, INC. LASERCATH (STERILE), Substantially Equivalent on 1986-04-07. Applicant: Hgm, Inc.. Device class: 2.

Clearance details

Applicant: Hgm, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1986-01-30
Decision date: 1986-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, 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 Hgm, Inc.

K950120 — SMART PLUG1995-08-11
K931072 — HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE1994-11-10
K931784 — HGM ILLUMINATING IMAGING ENDOCULAR PROBE1994-03-01
K933333 — HGM SCANMAN PLUS1993-09-23
K931499 — Q-11 OPHTHALMIC LASER1993-08-19

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