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FDA 510(k)

ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED

K-Number: K912328 · 1992-11-06

ApplicantAdvanced Rehabilitative Technology, Inc.
Decision Date1992-11-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Rehabilitative Technology, Inc.. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K912328. 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 ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED?

ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Advanced Rehabilitative Technology, Inc.. The 510(k) number is K912328.

When did ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED receive FDA 510(k) clearance?

ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED received FDA 510(k) clearance on 1992-11-06, under 510(k) number K912328.

Who is the listed applicant for ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED?

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

What is the FDA product code for ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED?

The FDA product code for ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED is IPF.

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Other records listing Advanced Rehabilitative Technology, 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.

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Official Source

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