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FDA 510(k)

FLOWSCAN

K-Number: K924413 · 1993-05-06

Decision Date1993-05-06
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOWSCAN is the device name listed in this FDA 510(k) record. The listed applicant is Electrocaine Medical System. It received FDA 510(k) clearance on 1993-05-06 under 510(k) number K924413. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOWSCAN?

FLOWSCAN is a medical device that received FDA 510(k) clearance on 1993-05-06. The listed applicant is Electrocaine Medical System. The 510(k) number is K924413.

When did FLOWSCAN receive FDA 510(k) clearance?

FLOWSCAN received FDA 510(k) clearance on 1993-05-06, under 510(k) number K924413.

Who is the listed applicant for FLOWSCAN?

The FDA 510(k) record lists Electrocaine Medical System as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOWSCAN?

The FDA product code for FLOWSCAN is BZG.

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 Electrocaine Medical System 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: BZG)

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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