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FDA 510(k)

LTDT PATIENT LIFTER

K-Number: K884110 · 1988-10-13

ApplicantDevine Medical Products
Decision Date1988-10-13
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LTDT PATIENT LIFTER is the device name listed in this FDA 510(k) record. The listed applicant is Devine Medical Products. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K884110. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LTDT PATIENT LIFTER?

LTDT PATIENT LIFTER is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Devine Medical Products. The 510(k) number is K884110.

When did LTDT PATIENT LIFTER receive FDA 510(k) clearance?

LTDT PATIENT LIFTER received FDA 510(k) clearance on 1988-10-13, under 510(k) number K884110.

Who is the listed applicant for LTDT PATIENT LIFTER?

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

What is the FDA product code for LTDT PATIENT LIFTER?

The FDA product code for LTDT PATIENT LIFTER is ILK.

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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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