ALLERGEN IMMUNDOCAP MODELC5, C6, C73, E201, E213, F50, F51,F54, F55, F56, F57, F58, F59, F60, F61, F205, F213, F218, F
FDA 510(k) clearance K993388 · decided 1999-12-01
Clearance details
- K-number
- K993388
- Device name
- ALLERGEN IMMUNDOCAP MODELC5, C6, C73, E201, E213, F50, F51,F54, F55, F56, F57, F58, F59, F60, F61, F205, F213, F218, F
- Applicant
- Pharmacia & Upjohn Co.
- Decision
- Substantially Equivalent
- Date received
- 1999-10-08
- Decision date
- 1999-12-01
- Days to decision
- 54 days
- Clearance type
- Traditional
- Product code
- DHB
- Device class
- 2
- Regulation number
- 866.5750
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- Location
- Westervillle, OH, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.