NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV
FDA 510(k) clearance K820334 · decided 1982-03-15
Clearance details
- K-number
- K820334
- Device name
- NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV
- Applicant
- Nemectron Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-02-05
- Decision date
- 1982-03-15
- Days to decision
- 38 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.