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FDA 510(k)

K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS)

K-Number: K973259 · 1997-09-10

ApplicantMedical Creative Technologies, Inc.
Decision Date1997-09-10
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Creative Technologies, Inc.. It received FDA 510(k) clearance on 1997-09-10 under 510(k) number K973259. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS)?

K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS) is a medical device that received FDA 510(k) clearance on 1997-09-10. The listed applicant is Medical Creative Technologies, Inc.. The 510(k) number is K973259.

When did K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS) receive FDA 510(k) clearance?

K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS) received FDA 510(k) clearance on 1997-09-10, under 510(k) number K973259.

Who is the listed applicant for K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS)?

The FDA 510(k) record lists Medical Creative Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS)?

The FDA product code for K&W 2-PIECE TAKE-APART INSTRUMENTS(VARIOUS) is OCZ.

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Other records listing Medical Creative Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: OCZ)

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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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