FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MDx-Chex for BCP
K Number: K260041
·
Decision Mar 27, 2026
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
30
Applicant Total
2
Review Days
80
Basic Information
- Device Name
- MDx-Chex for BCP
- K Number
- K260041
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3920
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Streck, LLC
- Date Received
- January 6, 2026
- Decision Date
- March 27, 2026
- Product Code
- PMN
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PMN | Assayed External Control Material For Microbiology Nucleic Acid Amplification (Nat) Assays | FDA class 2 | Microbiology |
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Other Clearances by Streck, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K254167 | MDx-Chex for BCY | Mar 17, 2026 | Substantially Equivalent |