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FDA 510(k)

NITINOL GENTLE TOUCH COIL SPRING

K-Number: K923839 · 1992-10-15

Decision Date1992-10-15
Product CodeDZC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NITINOL GENTLE TOUCH COIL SPRING is the device name listed in this FDA 510(k) record. The listed applicant is Ultimate Wireforms, Inc.. It received FDA 510(k) clearance on 1992-10-15 under 510(k) number K923839. 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 NITINOL GENTLE TOUCH COIL SPRING?

NITINOL GENTLE TOUCH COIL SPRING is a medical device that received FDA 510(k) clearance on 1992-10-15. The listed applicant is Ultimate Wireforms, Inc.. The 510(k) number is K923839.

When did NITINOL GENTLE TOUCH COIL SPRING receive FDA 510(k) clearance?

NITINOL GENTLE TOUCH COIL SPRING received FDA 510(k) clearance on 1992-10-15, under 510(k) number K923839.

Who is the listed applicant for NITINOL GENTLE TOUCH COIL SPRING?

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

What is the FDA product code for NITINOL GENTLE TOUCH COIL SPRING?

The FDA product code for NITINOL GENTLE TOUCH COIL SPRING 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 Ultimate Wireforms, 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.

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

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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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