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FDA 510(k)

PREMISE SERIES BED

K-Number: K890845 · 1989-06-15

ApplicantBatesville American Mfg. Co.
Decision Date1989-06-15
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PREMISE SERIES BED is the device name listed in this FDA 510(k) record. The listed applicant is Batesville American Mfg. Co.. It received FDA 510(k) clearance on 1989-06-15 under 510(k) number K890845. 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 PREMISE SERIES BED?

PREMISE SERIES BED is a medical device that received FDA 510(k) clearance on 1989-06-15. The listed applicant is Batesville American Mfg. Co.. The 510(k) number is K890845.

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

PREMISE SERIES BED received FDA 510(k) clearance on 1989-06-15, under 510(k) number K890845.

Who is the listed applicant for PREMISE SERIES BED?

The FDA 510(k) record lists Batesville American Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREMISE SERIES BED?

The FDA product code for PREMISE SERIES BED is FNL.

Related Clinical Trials

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 Batesville American Mfg. Co. 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.

K894296PREMISE SERIES BED

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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