VIBROMETRY SYSTEM
FDA 510(k) clearance K901881 · decided 1991-05-31
Clearance details
- K-number
- K901881
- Device name
- VIBROMETRY SYSTEM
- Applicant
- Bruel & Kjaer Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-04-26
- Decision date
- 1991-05-31
- Days to decision
- 400 days
- Clearance type
- Traditional
- Product code
- LNN
- Advisory committee
- Unknown
- Location
- Hoffman Estates, IL, 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 |
|---|---|---|
| MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER (K932342) | Victoreen, Inc. | 1993-12-13 |
Recalls involving this device
No recalls on record reference this clearance.