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FDA 510(k)

EVEREST & JENNING SERIES 5000 MODULAR BED

K-Number: K854832 · 1986-02-04

ApplicantCarrom Healthcare, Inc.
Decision Date1986-02-04
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EVEREST & JENNING SERIES 5000 MODULAR BED is the device name listed in this FDA 510(k) record. The listed applicant is Carrom Healthcare, Inc.. It received FDA 510(k) clearance on 1986-02-04 under 510(k) number K854832. 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 EVEREST & JENNING SERIES 5000 MODULAR BED?

EVEREST & JENNING SERIES 5000 MODULAR BED is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Carrom Healthcare, Inc.. The 510(k) number is K854832.

When did EVEREST & JENNING SERIES 5000 MODULAR BED receive FDA 510(k) clearance?

EVEREST & JENNING SERIES 5000 MODULAR BED received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854832.

Who is the listed applicant for EVEREST & JENNING SERIES 5000 MODULAR BED?

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

What is the FDA product code for EVEREST & JENNING SERIES 5000 MODULAR BED?

The FDA product code for EVEREST & JENNING SERIES 5000 MODULAR 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 Carrom Healthcare, 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.

K854867EVEREST & JENNINGS TRADITION-STANDARD BED L109684&K854937CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEMK854776EVEREST & JENNINGS BED MODEL NO. L109564 & L108564K853270CENTERCOM CONTROL

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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