VALLEY FORGE BIPOLAR LOOP— 510(k) K971986

Name: FDA 510(k) clearance K971986
Creator: U.S. Food and Drug Administration
Published: 1997-08-26

Substantially Equivalent

Valley Forge Scientific Corp.

FDA 510(k) clearance K971986 for VALLEY FORGE BIPOLAR LOOP, Substantially Equivalent on 1997-08-26. Applicant: Valley Forge Scientific Corp.. Device class: 2.

Clearance details

Applicant: Valley Forge Scientific Corp.
Product code: Code HGI
Device class: Class 2
Regulation: 21 CFR 884.4120
Advisory panel: Obstetrics/Gynecology
Date received: 1997-05-29
Decision date: 1997-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oaks, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HGI

view all

K202915 — IRIS Thermocoagulator and Digital Colposcope2021-04-23
K152843 — Liger Medical HTU-1102016-06-24
K130606 — FMWAND FERROMAGNETIC SURGICAL SYSTEM2014-01-03
K121881 — DOMAIN SURGICAL SYSTEM2012-10-18
K070877 — ENDOCERVICAL ELECTRODE # 22007-07-27

More clearances from Valley Forge Scientific Corp.

view all

K050364 — MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM2005-03-09
K042604 — VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTS2004-10-22
K032601 — STRYKER INTERVENTIONAL PAIN RF GENERATOR2004-04-01
K033499 — MALIS IRRIGATION MODULE 10002003-11-28
K982229 — BI-DENT1998-08-13

Adverse events under product code HGI

product code HGI

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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