FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGM (WB0400M)
K Number: K971007
·
Decision Jun 1, 1998
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
110
Applicant Total
7
Review Days
439
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Basic Information
- Device Name
- LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGM (WB0400M)
- K Number
- K971007
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3830
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Mrl Diagnostics
- Date Received
- March 19, 1997
- Decision Date
- June 1, 1998
- Product Code
- LSR
- 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 |
|---|---|---|---|
| LSR | Reagent, Borrelia Serological Reagent | FDA class 2 | Microbiology |
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Other Clearances by Mrl Diagnostics
| K Number | Device Name | ||
|---|---|---|---|
| K000238 | HSV-1 & HSV-2 DIFFERENTIATION IMMUNOBLOT IGG, MODEL IB0900G | Apr 14, 2000 | Substantially Equivalent |
| K993754 | HSV-1 ELISA IGG, MODEL EL0910G | Feb 9, 2000 | Substantially Equivalent |
| K993724 | HSV-2 ELISA IGG, MODEL EL0920G | Feb 1, 2000 | Substantially Equivalent |
| K971006 | LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGG (WB0400G) | Jun 1, 1998 | Substantially Equivalent |
| K946353 | EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN RECOMBINANT IMMUNOFLUORESCENT ASSAY | Jul 21, 1995 | Substantially Equivalent |
| K931520 | EPSTEIN-BARR VIRUS VCA (IGM) RECOMB IMMUN ANTIBODY | Apr 26, 1994 | Substantially Equivalent |