MEDGRAPHICS PF/DX
K-Number: K912906 · 1992-02-04
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Device Summary
Frequently Asked Questions
What is the MEDGRAPHICS PF/DX?
MEDGRAPHICS PF/DX is a medical device that received FDA 510(k) clearance on 1992-02-04. The listed applicant is Medical Graphics Corp.. The 510(k) number is K912906.
When did MEDGRAPHICS PF/DX receive FDA 510(k) clearance?
MEDGRAPHICS PF/DX received FDA 510(k) clearance on 1992-02-04, under 510(k) number K912906.
Who is the listed applicant for MEDGRAPHICS PF/DX?
The FDA 510(k) record lists Medical Graphics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDGRAPHICS PF/DX?
The FDA product code for MEDGRAPHICS PF/DX is BZL.
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 Medical Graphics 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.
Related Devices (Code: BZL)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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