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FDA 510(k)

QUICKIE & ZIPPIE SERIES

K-Number: K123975 · 2013-08-16

ApplicantSunrise Medical
Decision Date2013-08-16
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUICKIE & ZIPPIE SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical. It received FDA 510(k) clearance on 2013-08-16 under 510(k) number K123975. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKIE & ZIPPIE SERIES?

QUICKIE & ZIPPIE SERIES is a medical device that received FDA 510(k) clearance on 2013-08-16. The listed applicant is Sunrise Medical. The 510(k) number is K123975.

When did QUICKIE & ZIPPIE SERIES receive FDA 510(k) clearance?

QUICKIE & ZIPPIE SERIES received FDA 510(k) clearance on 2013-08-16, under 510(k) number K123975.

Who is the listed applicant for QUICKIE & ZIPPIE SERIES?

The FDA 510(k) record lists Sunrise Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICKIE & ZIPPIE SERIES?

The FDA product code for QUICKIE & ZIPPIE SERIES is IOR.

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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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