BLADE SAFE
K-Number: K810208 · 1981-02-12
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Device Summary
Frequently Asked Questions
What is the BLADE SAFE?
BLADE SAFE is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Instranetics, Inc.. The 510(k) number is K810208.
When did BLADE SAFE receive FDA 510(k) clearance?
BLADE SAFE received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810208.
Who is the listed applicant for BLADE SAFE?
The FDA 510(k) record lists Instranetics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLADE SAFE?
The FDA product code for BLADE SAFE is MMK.
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 Instranetics, 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: MMK)
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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