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FDA 510(k)

SERIES 7000

K-Number: K790456 · 1979-03-23

Decision Date1979-03-23
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERIES 7000 is the device name listed in this FDA 510(k) record. The listed applicant is Narco Mckesson Co.. It received FDA 510(k) clearance on 1979-03-23 under 510(k) number K790456. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 7000?

SERIES 7000 is a medical device that received FDA 510(k) clearance on 1979-03-23. The listed applicant is Narco Mckesson Co.. The 510(k) number is K790456.

When did SERIES 7000 receive FDA 510(k) clearance?

SERIES 7000 received FDA 510(k) clearance on 1979-03-23, under 510(k) number K790456.

Who is the listed applicant for SERIES 7000?

The FDA 510(k) record lists Narco Mckesson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 7000?

The FDA product code for SERIES 7000 is BSZ.

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 Narco Mckesson Co. 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: BSZ)

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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