LATEX (K82)
FDA 510(k) clearance K931746 · decided 1995-03-21
Clearance details
- K-number
- K931746
- Device name
- LATEX (K82)
- Applicant
- Diagnostic Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1993-04-08
- Decision date
- 1995-03-21
- Days to decision
- 712 days
- Clearance type
- Traditional
- Product code
- DHB
- Device class
- 2
- Regulation number
- 866.5750
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- Location
- Los Angeles, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.