PROMPT INOCULATION SYSTEM— 510(k) K820299
Substantially Equivalent3M Company
FDA 510(k) clearance K820299 for PROMPT INOCULATION SYSTEM, Substantially Equivalent on 1982-03-15. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code LIE
- Device class
- Class 2
- Regulation
- 21 CFR 866.1640
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- White City, OR, US
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Recalls naming K820299
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 K820299.
Data sourced from openFDA. This site is unofficial and independent of the FDA.