North Eos Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K963685 | EOS BRAND DISPOSABLE CYTO/CERVICAL SAMPLER | October 11, 1996 |
| K963377 | EOS BRAND DISPOSABLE VAGINAL SPECULUM-EOSSPEC | October 4, 1996 |
| K954614 | EOS BRAND DISPOSABLE PROCTOSCOPE | April 10, 1996 |