FDA 510(k)

MSI 5000 SERIES BED

K-Number: K881965 · 1988-05-31

Decision Date1988-05-31

Product CodeFNL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MSI 5000 SERIES BED is the device name listed in this FDA 510(k) record. The listed applicant is Med Service, Inc.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K881965. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSI 5000 SERIES BED?

MSI 5000 SERIES BED is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Med Service, Inc.. The 510(k) number is K881965.

When did MSI 5000 SERIES BED receive FDA 510(k) clearance?

MSI 5000 SERIES BED received FDA 510(k) clearance on 1988-05-31, under 510(k) number K881965.

Who is the listed applicant for MSI 5000 SERIES BED?

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

What is the FDA product code for MSI 5000 SERIES BED?

The FDA product code for MSI 5000 SERIES BED is FNL.

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Other records listing Med Service, Inc. as applicant

K881960MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74 K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64 K881782MSI 4000 SERIES BED K881964MSI 3003 SERIES BED K881963MSI 3002 SERIES BED K881962MSI 2005 SERIES BED

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Related Devices (Code: FNL)

K202964iBed Wireless with iBed MobileStryker Corporation K103536IBED WIRELESS WITH IBED AWARENESSStryker Corporation K982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, Inc.

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.