REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER
K-Number: K933378 · 1993-11-12
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Device Summary
Frequently Asked Questions
What is the REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER?
REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER 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 K933378.
When did REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER receive FDA 510(k) clearance?
REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER received FDA 510(k) clearance on 1993-11-12, under 510(k) number K933378.
Who is the listed applicant for REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER?
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 CURVE NITI ARCH WIRE REPACKER RELABETER?
The FDA product code for REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER 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.
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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