ZIPPIE 3 TS/SP WHEELCHAIR/STANDER
K-Number: K920463 · 1992-04-02
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Device Summary
Frequently Asked Questions
What is the ZIPPIE 3 TS/SP WHEELCHAIR/STANDER?
ZIPPIE 3 TS/SP WHEELCHAIR/STANDER is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is Sunrise Medical Quickie Designs, Inc.. The 510(k) number is K920463.
When did ZIPPIE 3 TS/SP WHEELCHAIR/STANDER receive FDA 510(k) clearance?
ZIPPIE 3 TS/SP WHEELCHAIR/STANDER received FDA 510(k) clearance on 1992-04-02, under 510(k) number K920463.
Who is the listed applicant for ZIPPIE 3 TS/SP WHEELCHAIR/STANDER?
The FDA 510(k) record lists Sunrise Medical Quickie Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZIPPIE 3 TS/SP WHEELCHAIR/STANDER?
The FDA product code for ZIPPIE 3 TS/SP WHEELCHAIR/STANDER is IPL.
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 Quickie Designs, 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: IPL)
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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