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FDA 510(k)

MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE

K-Number: K963704 · 1996-11-26

Decision Date1996-11-26
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE is the device name listed in this FDA 510(k) record. The listed applicant is Shippert Medical Technologies Corp.. It received FDA 510(k) clearance on 1996-11-26 under 510(k) number K963704. The device is classified under product code LYG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE?

MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE is a medical device that received FDA 510(k) clearance on 1996-11-26. The listed applicant is Shippert Medical Technologies Corp.. The 510(k) number is K963704.

When did MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE receive FDA 510(k) clearance?

MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE received FDA 510(k) clearance on 1996-11-26, under 510(k) number K963704.

Who is the listed applicant for MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE?

The FDA 510(k) record lists Shippert Medical Technologies Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE?

The FDA product code for MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE is LYG.

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 Shippert Medical Technologies Corp. 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.

View all 13 devices →

Related Devices (Code: LYG)

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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