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FDA 510(k)

MSI 3002 SERIES BED

K-Number: K881963 · 1988-06-28

ApplicantMed Service, Inc.
Decision Date1988-06-28
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MSI 3002 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 1988-06-28 under 510(k) number K881963. 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 3002 SERIES BED?

MSI 3002 SERIES BED is a medical device that received FDA 510(k) clearance on 1988-06-28. The listed applicant is Med Service, Inc.. The 510(k) number is K881963.

When did MSI 3002 SERIES BED receive FDA 510(k) clearance?

MSI 3002 SERIES BED received FDA 510(k) clearance on 1988-06-28, under 510(k) number K881963.

Who is the listed applicant for MSI 3002 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 3002 SERIES BED?

The FDA product code for MSI 3002 SERIES BED is FNL.

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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.

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Other records listing Med Service, Inc. as applicant

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.

K881960MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64K881782MSI 4000 SERIES BEDK881964MSI 3003 SERIES BEDK881962MSI 2005 SERIES BEDK881965MSI 5000 SERIES BED

View all 9 devices →

Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 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.

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