ZEE EXTRICATION DEVICE— 510(k) K812342
Substantially EquivalentZee Medical Products Co., Inc.
FDA 510(k) clearance K812342 for ZEE EXTRICATION DEVICE, Substantially Equivalent on 1981-09-21. Applicant: Zee Medical Products Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Zee Medical Products Co., Inc.
- Product code
- Code IQF
- Device class
- Class 1
- Regulation
- 21 CFR 890.3490
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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