510(k) K802891
- Device
- Argyle Double Seal Chest Drainage Unit
- Applicant
- SHERWOOD MEDICAL CO.
- 510(k) number
- K802891
- Product code
- CCJ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-12-19
- Date received
- 1980-11-17
- Regulation
- 868.1430
- Classification name
- Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3033509895
- 3002808458
- 3014023337
- 1223858
- 3005053770
- 3033959233
- 9612890
- 9615102
- 3002622685
- 3009896423
- 3008614998
Source Documents#
510(k) summary PDF not indicated by FDA
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