FDA 510(k)

LOCKING WIRE GUIDE STYLET

K-Number: K890820 · 1989-03-22

ApplicantMedical Engineering and Development Institute

Decision Date1989-03-22

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LOCKING WIRE GUIDE STYLET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering and Development Institute. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K890820. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCKING WIRE GUIDE STYLET?

LOCKING WIRE GUIDE STYLET is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Medical Engineering and Development Institute. The 510(k) number is K890820.

When did LOCKING WIRE GUIDE STYLET receive FDA 510(k) clearance?

LOCKING WIRE GUIDE STYLET received FDA 510(k) clearance on 1989-03-22, under 510(k) number K890820.

Who is the listed applicant for LOCKING WIRE GUIDE STYLET?

The FDA 510(k) record lists Medical Engineering and Development Institute as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOCKING WIRE GUIDE STYLET?

The FDA product code for LOCKING WIRE GUIDE STYLET is GAD.

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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.