ZIPPIE P500
K-Number: K920179 · 1992-04-29
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Device Summary
Frequently Asked Questions
What is the ZIPPIE P500?
ZIPPIE P500 is a medical device that received FDA 510(k) clearance on 1992-04-29. The listed applicant is Sunrise Medical Quickie Designs, Inc.. The 510(k) number is K920179.
When did ZIPPIE P500 receive FDA 510(k) clearance?
ZIPPIE P500 received FDA 510(k) clearance on 1992-04-29, under 510(k) number K920179.
Who is the listed applicant for ZIPPIE P500?
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 P500?
The FDA product code for ZIPPIE P500 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 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: 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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