CAPTIA(R) SYPHILIS-M
FDA 510(k) clearance K871548 · decided 1987-08-07
Clearance details
- K-number
- K871548
- Device name
- CAPTIA(R) SYPHILIS-M
- Applicant
- Mercia Diagnostics , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1987-04-20
- Decision date
- 1987-08-07
- Days to decision
- 109 days
- Clearance type
- Traditional
- Product code
- LIP
- Device class
- 2
- Regulation number
- 866.3830
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Guildford, Surrey England, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.