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FDA 510(k)

SAFARI

K-Number: K010606 · 2001-03-16

ApplicantRanger All Season Corp.
Decision Date2001-03-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SAFARI is the device name listed in this FDA 510(k) record. The listed applicant is Ranger All Season Corp.. It received FDA 510(k) clearance on 2001-03-16 under 510(k) number K010606. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFARI?

SAFARI is a medical device that received FDA 510(k) clearance on 2001-03-16. The listed applicant is Ranger All Season Corp.. The 510(k) number is K010606.

When did SAFARI receive FDA 510(k) clearance?

SAFARI received FDA 510(k) clearance on 2001-03-16, under 510(k) number K010606.

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

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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.

K011107MODIFICATION TO SOLOK970646SAFARIK970523SOLO

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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