FDA 510(k)

PARAGON 9000 TILT AND TURN BED

K-Number: K872923 · 1987-10-14

Decision Date1987-10-14

Product CodeFNL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PARAGON 9000 TILT AND TURN BED is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Med, Inc.. It received FDA 510(k) clearance on 1987-10-14 under 510(k) number K872923. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAGON 9000 TILT AND TURN BED?

PARAGON 9000 TILT AND TURN BED is a medical device that received FDA 510(k) clearance on 1987-10-14. The listed applicant is Surgi-Med, Inc.. The 510(k) number is K872923.

When did PARAGON 9000 TILT AND TURN BED receive FDA 510(k) clearance?

PARAGON 9000 TILT AND TURN BED received FDA 510(k) clearance on 1987-10-14, under 510(k) number K872923.

Who is the listed applicant for PARAGON 9000 TILT AND TURN BED?

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

What is the FDA product code for PARAGON 9000 TILT AND TURN BED?

The FDA product code for PARAGON 9000 TILT AND TURN BED is FNL.

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Other records listing Surgi-Med, Inc. as applicant

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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.