TUBE HOLDING DEVICE— 510(k) K770108
Substantially EquivalentPharmaseal Div., Baxter Healthcare Corp.
FDA 510(k) clearance K770108 for TUBE HOLDING DEVICE, Substantially Equivalent on 1977-03-10. Applicant: Pharmaseal Div., Baxter Healthcare Corp.. Device class: 2.
Clearance details
- Applicant
- Pharmaseal Div., Baxter Healthcare Corp.
- Product code
- Code FPK
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Pharmaseal Div., Baxter Healthcare Corp.
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