QUICKIE TSR
K-Number: K952641 · 1995-07-06
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Device Summary
Frequently Asked Questions
What is the QUICKIE TSR?
QUICKIE TSR is a medical device that received FDA 510(k) clearance on 1995-07-06. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K952641.
When did QUICKIE TSR receive FDA 510(k) clearance?
QUICKIE TSR received FDA 510(k) clearance on 1995-07-06, under 510(k) number K952641.
Who is the listed applicant for QUICKIE TSR?
The FDA 510(k) record lists Sunrise Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUICKIE TSR?
The FDA product code for QUICKIE TSR is IOR.
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 Sunrise Medical, 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: IOR)
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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