CONTACT TIPS
K-Number: K861955 · 1986-08-14
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Device Summary
Frequently Asked Questions
What is the CONTACT TIPS?
CONTACT TIPS is a medical device that received FDA 510(k) clearance on 1986-08-14. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K861955.
When did CONTACT TIPS receive FDA 510(k) clearance?
CONTACT TIPS received FDA 510(k) clearance on 1986-08-14, under 510(k) number K861955.
Who is the listed applicant for CONTACT TIPS?
The FDA 510(k) record lists Cooper Lasersonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTACT TIPS?
The FDA product code for CONTACT TIPS is LNK.
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 Cooper Lasersonics, 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: LNK)
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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