The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hp M1722a/b And M1723a/b Codemaster.
| Device ID | K944608 |
| 510k Number | K944608 |
| Device Name: | HP M1722A/B AND M1723A/B CODEMASTER |
| Classification | Oximeter |
| Applicant | HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville, OR 97128 |
| Contact | Nancy Winn |
| Correspondent | Nancy Winn HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville, OR 97128 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-09-19 |
| Decision Date | 1994-10-04 |