LINEAR VIBRATION A MCSHIRLEY PRODUCT
K-Number: K833370 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the LINEAR VIBRATION A MCSHIRLEY PRODUCT?
LINEAR VIBRATION A MCSHIRLEY PRODUCT is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Mcshirley Products, Inc.. The 510(k) number is K833370.
When did LINEAR VIBRATION A MCSHIRLEY PRODUCT receive FDA 510(k) clearance?
LINEAR VIBRATION A MCSHIRLEY PRODUCT received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833370.
Who is the listed applicant for LINEAR VIBRATION A MCSHIRLEY PRODUCT?
The FDA 510(k) record lists Mcshirley Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LINEAR VIBRATION A MCSHIRLEY PRODUCT?
The FDA product code for LINEAR VIBRATION A MCSHIRLEY PRODUCT is IRO.
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 Mcshirley Products, 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: IRO)
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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