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FDA 510(k)

STIMULATOR, ULTRASOUND AND MUSCLE

K-Number: K871647 · 1987-06-29

ApplicantAmy West
Decision Date1987-06-29
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

STIMULATOR, ULTRASOUND AND MUSCLE is the device name listed in this FDA 510(k) record. The listed applicant is Amy West. It received FDA 510(k) clearance on 1987-06-29 under 510(k) number K871647. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the STIMULATOR, ULTRASOUND AND MUSCLE?

STIMULATOR, ULTRASOUND AND MUSCLE is a medical device that received FDA 510(k) clearance on 1987-06-29. The listed applicant is Amy West. The 510(k) number is K871647.

When did STIMULATOR, ULTRASOUND AND MUSCLE receive FDA 510(k) clearance?

STIMULATOR, ULTRASOUND AND MUSCLE received FDA 510(k) clearance on 1987-06-29, under 510(k) number K871647.

Who is the listed applicant for STIMULATOR, ULTRASOUND AND MUSCLE?

The FDA 510(k) record lists Amy West as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMULATOR, ULTRASOUND AND MUSCLE?

The FDA product code for STIMULATOR, ULTRASOUND AND MUSCLE is IMG.

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Related Devices (Code: IMG)

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.

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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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