MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER
FDA 510(k) clearance K932342 · decided 1993-12-13
Clearance details
- K-number
- K932342
- Device name
- MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER
- Applicant
- Victoreen, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-05-14
- Decision date
- 1993-12-13
- Days to decision
- 213 days
- Clearance type
- Traditional
- Product code
- LNN
- Advisory committee
- Unknown
- Location
- Cleveland, OH, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| VIBROMETRY SYSTEM (K901881) | Bruel & Kjaer Instruments, Inc. | 1991-05-31 |
Recalls involving this device
No recalls on record reference this clearance.