CENTRAL CATHETER KIT— 510(k) K780673
Substantially EquivalentArgon Medical Corp.
FDA 510(k) clearance K780673 for CENTRAL CATHETER KIT, Substantially Equivalent on 1978-05-16. Applicant: Argon Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Argon Medical 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 Argon Medical Corp.
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