TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR
K-Number: K861739 · 1986-06-09
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Device Summary
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
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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