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FDA 510(k)

PB GRAPHICS PRINTER AND PB VIDEO DISPLAY

K-Number: K863248 · 1986-09-03

Decision Date1986-09-03
Product CodeCBQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PB GRAPHICS PRINTER AND PB VIDEO DISPLAY is the device name listed in this FDA 510(k) record. The listed applicant is Datex Division Instrumentarium Corp.. It received FDA 510(k) clearance on 1986-09-03 under 510(k) number K863248. The device is classified under product code CBQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PB GRAPHICS PRINTER AND PB VIDEO DISPLAY?

PB GRAPHICS PRINTER AND PB VIDEO DISPLAY is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K863248.

When did PB GRAPHICS PRINTER AND PB VIDEO DISPLAY receive FDA 510(k) clearance?

PB GRAPHICS PRINTER AND PB VIDEO DISPLAY received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863248.

Who is the listed applicant for PB GRAPHICS PRINTER AND PB VIDEO DISPLAY?

The FDA 510(k) record lists Datex Division Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PB GRAPHICS PRINTER AND PB VIDEO DISPLAY?

The FDA product code for PB GRAPHICS PRINTER AND PB VIDEO DISPLAY is CBQ.

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 Datex Division Instrumentarium 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.

View all 55 devices →

Related Devices (Code: CBQ)

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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