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FDA 510(k)

HANDI-MOVE

K-Number: K854461 · 1986-03-14

ApplicantT.F. Herceg, Inc.
Decision Date1986-03-14
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HANDI-MOVE is the device name listed in this FDA 510(k) record. The listed applicant is T.F. Herceg, Inc.. It received FDA 510(k) clearance on 1986-03-14 under 510(k) number K854461. 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 HANDI-MOVE?

HANDI-MOVE is a medical device that received FDA 510(k) clearance on 1986-03-14. The listed applicant is T.F. Herceg, Inc.. The 510(k) number is K854461.

When did HANDI-MOVE receive FDA 510(k) clearance?

HANDI-MOVE received FDA 510(k) clearance on 1986-03-14, under 510(k) number K854461.

Who is the listed applicant for HANDI-MOVE?

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

What is the FDA product code for HANDI-MOVE?

The FDA product code for HANDI-MOVE 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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