510(k) K791327
- Device
- Argyle Taussig Culture Catheter
- Applicant
- SHERWOOD MEDICAL CO.
- 510(k) number
- K791327
- Product code
- KTR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-08-22
- Date received
- 1979-07-16
- Regulation
- 874.4680
- Classification name
- Tube, Aspirating, Bronchoscope, Rigid
- Medical specialty
- Ear, Nose, Throat
- Review panel
- Ear, Nose, Throat
- 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#
- 9710524
- 3010041511
- 3011137372
- 8040233
Source Documents#
510(k) summary PDF not indicated by FDA