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FDA 510(k)

HP M1722A/B AND M1723A/B CODEMASTER

K-Number: K944608 · 1994-10-04

Decision Date1994-10-04
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP M1722A/B AND M1723A/B CODEMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K944608. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 230 devices →

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

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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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