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FDA 510(k)

RHEOLOGIC I

K-Number: K903711 · 1991-01-16

ApplicantAdvanced Rehabilitative Technology, Inc.
Decision Date1991-01-16
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RHEOLOGIC I 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 1991-01-16 under 510(k) number K903711. 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 RHEOLOGIC I?

RHEOLOGIC I is a medical device that received FDA 510(k) clearance on 1991-01-16. The listed applicant is Advanced Rehabilitative Technology, Inc.. The 510(k) number is K903711.

When did RHEOLOGIC I receive FDA 510(k) clearance?

RHEOLOGIC I received FDA 510(k) clearance on 1991-01-16, under 510(k) number K903711.

Who is the listed applicant for RHEOLOGIC I?

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 RHEOLOGIC I?

The FDA product code for RHEOLOGIC I 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.

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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.

K915369THE EQUALIZERK912328ELECTRONIC MUSCLE STIMULATORS, EXCEL II, MODIFIED

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.

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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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