FDA 510(k)

HEAD BED

K-Number: K060986 · 2006-07-11

Decision Date2006-07-11

Product CodeFRP

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HEAD BED is the device name listed in this FDA 510(k) record. The listed applicant is Steven H. Warnock, M.D.. It received FDA 510(k) clearance on 2006-07-11 under 510(k) number K060986. The device is classified under product code FRP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEAD BED?

HEAD BED is a medical device that received FDA 510(k) clearance on 2006-07-11. The listed applicant is Steven H. Warnock, M.D.. The 510(k) number is K060986.

When did HEAD BED receive FDA 510(k) clearance?

HEAD BED received FDA 510(k) clearance on 2006-07-11, under 510(k) number K060986.

Who is the listed applicant for HEAD BED?

The FDA 510(k) record lists Steven H. Warnock, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEAD BED?

The FDA product code for HEAD BED is FRP.

Related Devices (Code: FRP)

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.

K082367INFANT SLEEP BEANIELife Innovations, LLC K090284RES-Q INFANT WEDGE AND SLINGCr Enterprises, LLC K062143KOZY COMFORT INFANT POSITIONERAlfred E Mann Inst. For Biomedical Engineering K051300ROBIN HOOD VESTKamber Corporation K041996NIGHTFORMPlastic Surgery Solutions, LLC K003511KENDALL-LTP TURNER SAVE-A-LINEThe Ludlow Company LP

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.