MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE
K-Number: K963704 · 1996-11-26
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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