510(k) K792714
- Device
- PARA-PAK PVA
- Applicant
- MERIDIAN DIAGNOSTICS, INC.
- 510(k) number
- K792714
- Product code
- IFQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-01-24
- Date received
- 1979-12-27
- Regulation
- 864.4010
- Classification name
- Formulations, Mercuric Chloride For Tissue
- Medical specialty
- Pathology
- Review panel
- Pathology
- Clearance type
- Traditional
- Third party reviewed
- No
Other 510(k) Records For Product Code IFQ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K792654 | CULTURETTE BRAND-PVA/FORMALIN KIT | Marion Laboratories, Inc. | 1980-01-24 |
Legacy Summary#
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FDA Review#
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