PARA-PAK CLEAN VIAL— 510(k) K792710
Substantially EquivalentMeridian Diagnostics, Inc.
FDA 510(k) clearance K792710 for PARA-PAK CLEAN VIAL, Substantially Equivalent on 1980-01-28. Applicant: Meridian Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- Meridian Diagnostics, Inc.
- Product code
- Code FMH
- Device class
- Class 1
- Regulation
- 21 CFR 864.3250
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code FMH
view allMore clearances from Meridian Diagnostics, Inc.
view allRecalls naming K792710
K-number listed on FDA's recall record- Z-0519-2024 — Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312
- Z-0521-2024 — Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: CHB900312
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K792710.
Data sourced from openFDA. This site is unofficial and independent of the FDA.