NITINOL GENTLE TOUCH COIL SPRING
K-Number: K923839 · 1992-10-15
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Device Summary
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
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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