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FDA 510(k)

VALLEY FORGE BIPOLAR BALL TIP ELECTRODE

K-Number: K973554 · 1997-12-19

ApplicantValley Forge Scientific Corp.
Decision Date1997-12-19
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEY FORGE BIPOLAR BALL TIP ELECTRODE 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 1997-12-19 under 510(k) number K973554. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEY FORGE BIPOLAR BALL TIP ELECTRODE?

VALLEY FORGE BIPOLAR BALL TIP ELECTRODE is a medical device that received FDA 510(k) clearance on 1997-12-19. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K973554.

When did VALLEY FORGE BIPOLAR BALL TIP ELECTRODE receive FDA 510(k) clearance?

VALLEY FORGE BIPOLAR BALL TIP ELECTRODE received FDA 510(k) clearance on 1997-12-19, under 510(k) number K973554.

Who is the listed applicant for VALLEY FORGE BIPOLAR BALL TIP ELECTRODE?

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 BALL TIP ELECTRODE?

The FDA product code for VALLEY FORGE BIPOLAR BALL TIP ELECTRODE is JOS.

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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-DENTK971986VALLEY FORGE BIPOLAR LOOP

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Related Devices (Code: JOS)

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K161600Resection ElectrodesOlympus Winter & Ibe GmbHK050923LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATORConmed LinvatecK012684REPROCESSED ELECTROSURGICAL ELECTRODESterilmed, Inc.K011515MEDLINE GROUNDING PADMedline Industries, Inc.K003403ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999Highland / Marietta, Inc.K000333STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MODTriad Surgical Technologies, 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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