SEDIPLAST— 510(k) K840500
Substantially EquivalentPrecision Technology, Inc.
FDA 510(k) clearance K840500 for SEDIPLAST, Substantially Equivalent on 1984-02-21. Applicant: Precision Technology, Inc.. Device class: 1.
Clearance details
- Applicant
- Precision Technology, Inc.
- Product code
- Product code JPH
- Device class
- Class 1
- Regulation
- 21 CFR 864.6700
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code JPH
view allMore clearances from Precision Technology, Inc.
view allRecalls naming K840500
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K840500.
Data sourced from openFDA. This site is unofficial and independent of the FDA.