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FDA 510(k)

CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC

K-Number: K022387 · 2002-09-19

ApplicantCraftmatic Organization, Inc.
Decision Date2002-09-19
Product CodeLLI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC is the device name listed in this FDA 510(k) record. The listed applicant is Craftmatic Organization, Inc.. It received FDA 510(k) clearance on 2002-09-19 under 510(k) number K022387. 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 ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC?

CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is Craftmatic Organization, Inc.. The 510(k) number is K022387.

When did CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC receive FDA 510(k) clearance?

CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022387.

Who is the listed applicant for CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC?

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

What is the FDA product code for CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC?

The FDA product code for CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC 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.

K840787CRAFTMATIC ELECTRIC ADJUSTABLE BEDContour, 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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