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FDA 510(k)

VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &

K-Number: K853992 · 1986-02-21

ApplicantValley Forge Scientific Corp.
Decision Date1986-02-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & 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 1986-02-21 under 510(k) number K853992. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &?

VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & is a medical device that received FDA 510(k) clearance on 1986-02-21. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K853992.

When did VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & receive FDA 510(k) clearance?

VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & received FDA 510(k) clearance on 1986-02-21, under 510(k) number K853992.

Who is the listed applicant for VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &?

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 SCIEN-TENS UNIT & ACCESS. LEAD WIRE &?

The FDA product code for VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & is GZJ.

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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: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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