FDA 510(k)

MSI STANDARD BED MODELS: L1097-64 AND L1085-64

K-Number: K881961 · 1988-11-01

Decision Date1988-11-01

Product CodeFNJ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MSI STANDARD BED MODELS: L1097-64 AND L1085-64 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 1988-11-01 under 510(k) number K881961. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSI STANDARD BED MODELS: L1097-64 AND L1085-64?

MSI STANDARD BED MODELS: L1097-64 AND L1085-64 is a medical device that received FDA 510(k) clearance on 1988-11-01. The listed applicant is Med Service, Inc.. The 510(k) number is K881961.

When did MSI STANDARD BED MODELS: L1097-64 AND L1085-64 receive FDA 510(k) clearance?

MSI STANDARD BED MODELS: L1097-64 AND L1085-64 received FDA 510(k) clearance on 1988-11-01, under 510(k) number K881961.

Who is the listed applicant for MSI STANDARD BED MODELS: L1097-64 AND L1085-64?

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 STANDARD BED MODELS: L1097-64 AND L1085-64?

The FDA product code for MSI STANDARD BED MODELS: L1097-64 AND L1085-64 is FNJ.

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Other records listing Med Service, Inc. as applicant

K881960MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74 K881782MSI 4000 SERIES BED K881963MSI 3002 SERIES BED K881964MSI 3003 SERIES BED K881962MSI 2005 SERIES BED K881965MSI 5000 SERIES BED

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Related Devices (Code: FNJ)

K934298KING KRIBNoritage, Inc.K892877CRADLE, HOSPITAL BED CLOTHINGWarsaw Orthopedic, Inc.K885241BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MATKing Mfg. Co.K884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDCommercial Products & Engineering Co.K881725ENVIROTENT (BED)Envirotents, Inc.K881964MSI 3003 SERIES BEDMed Service, 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.