ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR
FDA 510(k) clearance K852018 · decided 1985-07-11
Clearance details
- K-number
- K852018
- Device name
- ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR
- Applicant
- Manan Manufacturing Co., Inc.
- Decision
- Unknown
- Date received
- 1985-05-08
- Decision date
- 1985-07-11
- Days to decision
- 64 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Skokie, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.