FDA 510(k)

SOLOLIFT - PATIENT TRANSFER STRETCHER

K-Number: K871475 · 1987-05-11

Decision Date1987-05-11

Product CodeFMR

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SOLOLIFT - PATIENT TRANSFER STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Adel Medical , Ltd.. It received FDA 510(k) clearance on 1987-05-11 under 510(k) number K871475. The device is classified under product code FMR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLOLIFT - PATIENT TRANSFER STRETCHER?

SOLOLIFT - PATIENT TRANSFER STRETCHER is a medical device that received FDA 510(k) clearance on 1987-05-11. The listed applicant is Adel Medical , Ltd.. The 510(k) number is K871475.

When did SOLOLIFT - PATIENT TRANSFER STRETCHER receive FDA 510(k) clearance?

SOLOLIFT - PATIENT TRANSFER STRETCHER received FDA 510(k) clearance on 1987-05-11, under 510(k) number K871475.

Who is the listed applicant for SOLOLIFT - PATIENT TRANSFER STRETCHER?

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

What is the FDA product code for SOLOLIFT - PATIENT TRANSFER STRETCHER?

The FDA product code for SOLOLIFT - PATIENT TRANSFER STRETCHER is FMR.

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Other records listing Adel Medical , Ltd. as applicant

K890476ADEL - MODEL 986 INFANT WARMER K874610ADEL MODEL 2100 BIRTHING BED K861030LABOR-DELIVERY STRETCH/BED K860020MINOR SURGERY LIGHT MODEL 2112 K833321LABOR/DELIVERY/RECOVERY BED LDR-600 K810886ADEL MEDICAL BIRTHING BED, #LD-500

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Related Devices (Code: FMR)

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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.