SAFARI
K-Number: K970646 · 1997-08-25
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Device Summary
Frequently Asked Questions
What is the SAFARI?
SAFARI is a medical device that received FDA 510(k) clearance on 1997-08-25. The listed applicant is Ranger All Season Corp.. The 510(k) number is K970646.
When did SAFARI receive FDA 510(k) clearance?
SAFARI received FDA 510(k) clearance on 1997-08-25, under 510(k) number K970646.
Who is the listed applicant for SAFARI?
The FDA 510(k) record lists Ranger All Season Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAFARI?
The FDA product code for SAFARI is INI.
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 Ranger All Season Corp. 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: INI)
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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