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FDA 510(k)

SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH

K-Number: K891458 · 1989-10-20

ApplicantBack IN Action, Inc.
Decision Date1989-10-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH is the device name listed in this FDA 510(k) record. The listed applicant is Back IN Action, Inc.. It received FDA 510(k) clearance on 1989-10-20 under 510(k) number K891458. 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 SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH?

SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH is a medical device that received FDA 510(k) clearance on 1989-10-20. The listed applicant is Back IN Action, Inc.. The 510(k) number is K891458.

When did SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH receive FDA 510(k) clearance?

SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH received FDA 510(k) clearance on 1989-10-20, under 510(k) number K891458.

Who is the listed applicant for SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH?

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

What is the FDA product code for SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH?

The FDA product code for SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH 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 Back IN Action, 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.

K891394PM830 ELECTRIC MASSAGER

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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