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FDA 510(k)

DR. VOLKNER'S LAMELLAR TURNING BED(TM)

K-Number: K891457 · 1989-06-20

ApplicantJames Consolidated, Inc.
Decision Date1989-06-20
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DR. VOLKNER'S LAMELLAR TURNING BED(TM) is the device name listed in this FDA 510(k) record. The listed applicant is James Consolidated, Inc.. It received FDA 510(k) clearance on 1989-06-20 under 510(k) number K891457. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. VOLKNER'S LAMELLAR TURNING BED(TM)?

DR. VOLKNER'S LAMELLAR TURNING BED(TM) is a medical device that received FDA 510(k) clearance on 1989-06-20. The listed applicant is James Consolidated, Inc.. The 510(k) number is K891457.

When did DR. VOLKNER'S LAMELLAR TURNING BED(TM) receive FDA 510(k) clearance?

DR. VOLKNER'S LAMELLAR TURNING BED(TM) received FDA 510(k) clearance on 1989-06-20, under 510(k) number K891457.

Who is the listed applicant for DR. VOLKNER'S LAMELLAR TURNING BED(TM)?

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

What is the FDA product code for DR. VOLKNER'S LAMELLAR TURNING BED(TM)?

The FDA product code for DR. VOLKNER'S LAMELLAR TURNING BED(TM) is FNM.

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Related Devices (Code: FNM)

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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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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