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FDA 510(k)

VALLEY FORGE BIPOLAR LOOP

K-Number: K971986 · 1997-08-26

ApplicantValley Forge Scientific Corp.
Decision Date1997-08-26
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VALLEY FORGE BIPOLAR LOOP is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 1997-08-26 under 510(k) number K971986. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEY FORGE BIPOLAR LOOP?

VALLEY FORGE BIPOLAR LOOP is a medical device that received FDA 510(k) clearance on 1997-08-26. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K971986.

When did VALLEY FORGE BIPOLAR LOOP receive FDA 510(k) clearance?

VALLEY FORGE BIPOLAR LOOP received FDA 510(k) clearance on 1997-08-26, under 510(k) number K971986.

Who is the listed applicant for VALLEY FORGE BIPOLAR LOOP?

The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALLEY FORGE BIPOLAR LOOP?

The FDA product code for VALLEY FORGE BIPOLAR LOOP is HGI.

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Other records listing Valley Forge Scientific Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMK042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSK032601STRYKER INTERVENTIONAL PAIN RF GENERATORK033499MALIS IRRIGATION MODULE 1000K982229BI-DENTK973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODE

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Related Devices (Code: HGI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K022593THOMAS MEDICAL ELECTRODESThomas Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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