INJECT-SNARE
K-Number: K942110 · 1994-10-13
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Device Summary
Frequently Asked Questions
What is the INJECT-SNARE?
INJECT-SNARE is a medical device that received FDA 510(k) clearance on 1994-10-13. The listed applicant is Endovations. The 510(k) number is K942110.
When did INJECT-SNARE receive FDA 510(k) clearance?
INJECT-SNARE received FDA 510(k) clearance on 1994-10-13, under 510(k) number K942110.
Who is the listed applicant for INJECT-SNARE?
The FDA 510(k) record lists Endovations as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INJECT-SNARE?
The FDA product code for INJECT-SNARE is FDI.
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 Endovations 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: FDI)
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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