FDA 510(k)

SURGICAL WIRE CUTTERS

K-Number: K890250 · 1989-01-27

Decision Date1989-01-27

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SURGICAL WIRE CUTTERS is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Medical Products. It received FDA 510(k) clearance on 1989-01-27 under 510(k) number K890250. 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 SURGICAL WIRE CUTTERS?

SURGICAL WIRE CUTTERS is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Kinetic Medical Products. The 510(k) number is K890250.

When did SURGICAL WIRE CUTTERS receive FDA 510(k) clearance?

SURGICAL WIRE CUTTERS received FDA 510(k) clearance on 1989-01-27, under 510(k) number K890250.

Who is the listed applicant for SURGICAL WIRE CUTTERS?

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

What is the FDA product code for SURGICAL WIRE CUTTERS?

The FDA product code for SURGICAL WIRE CUTTERS is GAD.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.