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FDA 510(k)

ACU-MASSAGE TABLE

K-Number: K822693 · 1982-09-21

ApplicantH.W.E., Inc.
Decision Date1982-09-21
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACU-MASSAGE TABLE is the device name listed in this FDA 510(k) record. The listed applicant is H.W.E., Inc.. It received FDA 510(k) clearance on 1982-09-21 under 510(k) number K822693. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACU-MASSAGE TABLE?

ACU-MASSAGE TABLE is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is H.W.E., Inc.. The 510(k) number is K822693.

When did ACU-MASSAGE TABLE receive FDA 510(k) clearance?

ACU-MASSAGE TABLE received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822693.

Who is the listed applicant for ACU-MASSAGE TABLE?

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

What is the FDA product code for ACU-MASSAGE TABLE?

The FDA product code for ACU-MASSAGE TABLE is JFB.

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.

Related Devices (Code: JFB)

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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