MYOSURE ROD LENS SCOPE SEALS
K-Number: K102686 · 2010-10-15
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Device Summary
Frequently Asked Questions
What is the MYOSURE ROD LENS SCOPE SEALS?
MYOSURE ROD LENS SCOPE SEALS is a medical device that received FDA 510(k) clearance on 2010-10-15. The listed applicant is Interlace Medical, Inc.. The 510(k) number is K102686.
When did MYOSURE ROD LENS SCOPE SEALS receive FDA 510(k) clearance?
MYOSURE ROD LENS SCOPE SEALS received FDA 510(k) clearance on 2010-10-15, under 510(k) number K102686.
Who is the listed applicant for MYOSURE ROD LENS SCOPE SEALS?
The FDA 510(k) record lists Interlace Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYOSURE ROD LENS SCOPE SEALS?
The FDA product code for MYOSURE ROD LENS SCOPE SEALS is HIH.
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 Interlace Medical, 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: HIH)
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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