HP M1722A/B AND M1723A/B CODEMASTER
K-Number: K944608 · 1994-10-04
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Device Summary
Frequently Asked Questions
What is the HP M1722A/B AND M1723A/B CODEMASTER?
HP M1722A/B AND M1723A/B CODEMASTER is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K944608.
When did HP M1722A/B AND M1723A/B CODEMASTER receive FDA 510(k) clearance?
HP M1722A/B AND M1723A/B CODEMASTER received FDA 510(k) clearance on 1994-10-04, under 510(k) number K944608.
Who is the listed applicant for HP M1722A/B AND M1723A/B CODEMASTER?
The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HP M1722A/B AND M1723A/B CODEMASTER?
The FDA product code for HP M1722A/B AND M1723A/B CODEMASTER is DQA.
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 Hewlett-Packard 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: DQA)
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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