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FDA 510(k)

PORTA-PULS MUSCLE STIMULATOR

K-Number: K810244 · 1981-02-26

Decision Date1981-02-26
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTA-PULS MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is General Physiotherapy, Inc.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810244. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTA-PULS MUSCLE STIMULATOR?

PORTA-PULS MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is General Physiotherapy, Inc.. The 510(k) number is K810244.

When did PORTA-PULS MUSCLE STIMULATOR receive FDA 510(k) clearance?

PORTA-PULS MUSCLE STIMULATOR received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810244.

Who is the listed applicant for PORTA-PULS MUSCLE STIMULATOR?

The FDA 510(k) record lists General Physiotherapy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTA-PULS MUSCLE STIMULATOR?

The FDA product code for PORTA-PULS MUSCLE STIMULATOR is IRO.

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 General Physiotherapy, Inc. 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.

View all 9 devices →

Related Devices (Code: IRO)

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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