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FDA 510(k)

SPECTRASTIM 2000 MUSCLE STIMULATOR

K-Number: K900029 · 1990-04-02

Decision Date1990-04-02
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPECTRASTIM 2000 MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Therapeutic Technologies, Inc.. It received FDA 510(k) clearance on 1990-04-02 under 510(k) number K900029. 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 SPECTRASTIM 2000 MUSCLE STIMULATOR?

SPECTRASTIM 2000 MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is Therapeutic Technologies, Inc.. The 510(k) number is K900029.

When did SPECTRASTIM 2000 MUSCLE STIMULATOR receive FDA 510(k) clearance?

SPECTRASTIM 2000 MUSCLE STIMULATOR received FDA 510(k) clearance on 1990-04-02, under 510(k) number K900029.

Who is the listed applicant for SPECTRASTIM 2000 MUSCLE STIMULATOR?

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

What is the FDA product code for SPECTRASTIM 2000 MUSCLE STIMULATOR?

The FDA product code for SPECTRASTIM 2000 MUSCLE 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 Therapeutic Technologies, 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.

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

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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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