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FDA 510(k)

TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR

K-Number: K861739 · 1986-06-09

Decision Date1986-06-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is J.A. Preston Corp.. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K861739. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR?

TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is J.A. Preston Corp.. The 510(k) number is K861739.

When did TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR receive FDA 510(k) clearance?

TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR received FDA 510(k) clearance on 1986-06-09, under 510(k) number K861739.

Who is the listed applicant for TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR?

The FDA 510(k) record lists J.A. Preston Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR?

The FDA product code for TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR is IPF.

Related Clinical Trials

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.

Other records listing J.A. Preston 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.

Related Devices (Code: IPF)

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.

Official Source

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

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