HP M1722A/B AND M1723A/B CODEMASTER— 510(k) K944608
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K944608 for HP M1722A/B AND M1723A/B CODEMASTER, Substantially Equivalent on 1994-10-04. Applicant: Hewlett-Packard Co.. Device class: 2.
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code DQA
- Device class
- Class 2
- Regulation
- 21 CFR 870.2700
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mcminnville, OR, US
Recent devices under product code DQA
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- K252448 — AViTA Pulse Oximeter (SP61)
More clearances from Hewlett-Packard Co.
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- K993587 — HP M2376A DEVICE LINK SYSTEM
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- K992977 — HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504A
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Adverse events under product code DQA
product code DQA- Death
- 66
- Malfunction
- 2,867
- Other
- 1
- Total
- 2,934
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.