ASPIRATOR & PROBE, CYTOLOGY, ENDOMET.— 510(k) K772121
Substantially EquivalentSmithkline Diagnostics, Inc.
FDA 510(k) clearance K772121 for ASPIRATOR & PROBE, CYTOLOGY, ENDOMET., Substantially Equivalent on 1977-11-17. Applicant: Smithkline Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Smithkline Diagnostics, Inc.
- Product code
- Code HHK
- Device class
- Class 2
- Regulation
- 21 CFR 884.1175
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code HHK
view allMore clearances from Smithkline Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.