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FDA 510(k)

BEST MODEL # 81-01 SERIES IR-192 SOURCES

K-Number: K042786 · 2004-11-18

ApplicantBest Medical International, Inc.
Decision Date2004-11-18
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEST MODEL # 81-01 SERIES IR-192 SOURCES is the device name listed in this FDA 510(k) record. The listed applicant is Best Medical International, Inc.. It received FDA 510(k) clearance on 2004-11-18 under 510(k) number K042786. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEST MODEL # 81-01 SERIES IR-192 SOURCES?

BEST MODEL # 81-01 SERIES IR-192 SOURCES is a medical device that received FDA 510(k) clearance on 2004-11-18. The listed applicant is Best Medical International, Inc.. The 510(k) number is K042786.

When did BEST MODEL # 81-01 SERIES IR-192 SOURCES receive FDA 510(k) clearance?

BEST MODEL # 81-01 SERIES IR-192 SOURCES received FDA 510(k) clearance on 2004-11-18, under 510(k) number K042786.

Who is the listed applicant for BEST MODEL # 81-01 SERIES IR-192 SOURCES?

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

What is the FDA product code for BEST MODEL # 81-01 SERIES IR-192 SOURCES?

The FDA product code for BEST MODEL # 81-01 SERIES IR-192 SOURCES is KXK.

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Other records listing Best Medical International, 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.

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Related Devices (Code: KXK)

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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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