PERIPHERAL PULSE FUNCTION BLOCKS
FDA 510(k) clearance K810171 · decided 1981-02-25
Clearance details
- K-number
- K810171
- Device name
- PERIPHERAL PULSE FUNCTION BLOCKS
- Applicant
- Honeywell, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1981-01-22
- Decision date
- 1981-02-25
- Days to decision
- 34 days
- Clearance type
- Traditional
- Product code
- DSK
- Device class
- 2
- Regulation number
- 870.1110
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.