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FDA 510(k)

REVERSE SURVE NITI ARCH WIRE

K-Number: K933380 · 1993-11-12

Decision Date1993-11-12
Product CodeDZC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REVERSE SURVE NITI ARCH WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Highland Metals. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K933380. The device is classified under product code DZC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVERSE SURVE NITI ARCH WIRE?

REVERSE SURVE NITI ARCH WIRE is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Highland Metals. The 510(k) number is K933380.

When did REVERSE SURVE NITI ARCH WIRE receive FDA 510(k) clearance?

REVERSE SURVE NITI ARCH WIRE received FDA 510(k) clearance on 1993-11-12, under 510(k) number K933380.

Who is the listed applicant for REVERSE SURVE NITI ARCH WIRE?

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

What is the FDA product code for REVERSE SURVE NITI ARCH WIRE?

The FDA product code for REVERSE SURVE NITI ARCH WIRE is DZC.

Related Clinical Trials

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.

Other records listing Highland Metals 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.

View all 7 devices →

Related Devices (Code: DZC)

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.

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.

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