WIRE TWISTERS
K-Number: K830721 · 1983-04-12
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Device Summary
Frequently Asked Questions
What is the WIRE TWISTERS?
WIRE TWISTERS is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K830721.
When did WIRE TWISTERS receive FDA 510(k) clearance?
WIRE TWISTERS received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830721.
Who is the listed applicant for WIRE TWISTERS?
The FDA 510(k) record lists The Anspach Effort, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WIRE TWISTERS?
The FDA product code for WIRE TWISTERS is HTC.
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 The Anspach Effort, 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: HTC)
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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