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FDA 510(k)

EVEREST & JENNINGS TRADITION-STANDARD BED L109684&

K-Number: K854867 · 1986-02-04

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

Device Summary

EVEREST & JENNINGS TRADITION-STANDARD BED L109684& 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 K854867. 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 & JENNINGS TRADITION-STANDARD BED L109684&?

EVEREST & JENNINGS TRADITION-STANDARD BED L109684& 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 K854867.

When did EVEREST & JENNINGS TRADITION-STANDARD BED L109684& receive FDA 510(k) clearance?

EVEREST & JENNINGS TRADITION-STANDARD BED L109684& received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854867.

Who is the listed applicant for EVEREST & JENNINGS TRADITION-STANDARD BED L109684&?

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 & JENNINGS TRADITION-STANDARD BED L109684&?

The FDA product code for EVEREST & JENNINGS TRADITION-STANDARD BED L109684& is FNL.

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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.

K854832EVEREST & JENNING SERIES 5000 MODULAR BEDK854937CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEMK854776EVEREST & JENNINGS BED MODEL NO. L109564 & L108564K853270CENTERCOM CONTROL

Related Devices (Code: FNL)

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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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