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FDA 510(k)

CRAFTMATIC ELECTRIC ADJUSTABLE BED

K-Number: K840787 · 1984-06-13

ApplicantContour, Inc.
Decision Date1984-06-13
Product CodeLLI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRAFTMATIC ELECTRIC ADJUSTABLE BED is the device name listed in this FDA 510(k) record. The listed applicant is Contour, Inc.. It received FDA 510(k) clearance on 1984-06-13 under 510(k) number K840787. The device is classified under product code LLI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRAFTMATIC ELECTRIC ADJUSTABLE BED?

CRAFTMATIC ELECTRIC ADJUSTABLE BED is a medical device that received FDA 510(k) clearance on 1984-06-13. The listed applicant is Contour, Inc.. The 510(k) number is K840787.

When did CRAFTMATIC ELECTRIC ADJUSTABLE BED receive FDA 510(k) clearance?

CRAFTMATIC ELECTRIC ADJUSTABLE BED received FDA 510(k) clearance on 1984-06-13, under 510(k) number K840787.

Who is the listed applicant for CRAFTMATIC ELECTRIC ADJUSTABLE BED?

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

What is the FDA product code for CRAFTMATIC ELECTRIC ADJUSTABLE BED?

The FDA product code for CRAFTMATIC ELECTRIC ADJUSTABLE BED is LLI.

Related Clinical Trials

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Related Devices (Code: LLI)

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.

K022387CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSICCraftmatic Organization, 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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