FDA 510(k)

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED

K-Number: K121929 · 2013-01-17

Decision Date2013-01-17

Product CodeFRZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED is the device name listed in this FDA 510(k) record. The listed applicant is Diacor, Inc.. It received FDA 510(k) clearance on 2013-01-17 under 510(k) number K121929. The device is classified under product code FRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEPHYR 'X-SERIES PATIENT TRANSFER SLED?

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED is a medical device that received FDA 510(k) clearance on 2013-01-17. The listed applicant is Diacor, Inc.. The 510(k) number is K121929.

When did ZEPHYR 'X-SERIES PATIENT TRANSFER SLED receive FDA 510(k) clearance?

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED received FDA 510(k) clearance on 2013-01-17, under 510(k) number K121929.

Who is the listed applicant for ZEPHYR 'X-SERIES PATIENT TRANSFER SLED?

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

What is the FDA product code for ZEPHYR 'X-SERIES PATIENT TRANSFER SLED?

The FDA product code for ZEPHYR 'X-SERIES PATIENT TRANSFER SLED is FRZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.