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FDA 510(k)

THRUST-AIRE MODEL 2001

K-Number: K860618 · 1986-04-10

Decision Date1986-04-10
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

THRUST-AIRE MODEL 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Charron Industries, Inc.. It received FDA 510(k) clearance on 1986-04-10 under 510(k) number K860618. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the THRUST-AIRE MODEL 2001?

THRUST-AIRE MODEL 2001 is a medical device that received FDA 510(k) clearance on 1986-04-10. The listed applicant is Charron Industries, Inc.. The 510(k) number is K860618.

When did THRUST-AIRE MODEL 2001 receive FDA 510(k) clearance?

THRUST-AIRE MODEL 2001 received FDA 510(k) clearance on 1986-04-10, under 510(k) number K860618.

Who is the listed applicant for THRUST-AIRE MODEL 2001?

The FDA 510(k) record lists Charron Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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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