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FDA 510(k)

FOX BED MODEL 2001

K-Number: K854154 · 1985-11-08

ApplicantAce Mfg.
Decision Date1985-11-08
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FOX BED MODEL 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Ace Mfg.. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K854154. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOX BED MODEL 2001?

FOX BED MODEL 2001 is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Ace Mfg.. The 510(k) number is K854154.

When did FOX BED MODEL 2001 receive FDA 510(k) clearance?

FOX BED MODEL 2001 received FDA 510(k) clearance on 1985-11-08, under 510(k) number K854154.

Who is the listed applicant for FOX BED MODEL 2001?

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

What is the FDA product code for FOX BED MODEL 2001?

The FDA product code for FOX BED MODEL 2001 is FTC.

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.

Related Devices (Code: FTC)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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