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FDA 510(k)

THE KAUFMANN LIFT-AND-TURN MATTRESS

K-Number: K915306 · 1993-01-27

ApplicantKaufmann Sjukvardsartiklar
Decision Date1993-01-27
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE KAUFMANN LIFT-AND-TURN MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Kaufmann Sjukvardsartiklar. It received FDA 510(k) clearance on 1993-01-27 under 510(k) number K915306. 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 THE KAUFMANN LIFT-AND-TURN MATTRESS?

THE KAUFMANN LIFT-AND-TURN MATTRESS is a medical device that received FDA 510(k) clearance on 1993-01-27. The listed applicant is Kaufmann Sjukvardsartiklar. The 510(k) number is K915306.

When did THE KAUFMANN LIFT-AND-TURN MATTRESS receive FDA 510(k) clearance?

THE KAUFMANN LIFT-AND-TURN MATTRESS received FDA 510(k) clearance on 1993-01-27, under 510(k) number K915306.

Who is the listed applicant for THE KAUFMANN LIFT-AND-TURN MATTRESS?

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

What is the FDA product code for THE KAUFMANN LIFT-AND-TURN MATTRESS?

The FDA product code for THE KAUFMANN LIFT-AND-TURN MATTRESS is FNM.

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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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