USA ASPIRATOR
FDA 510(k) clearance K862751 · decided 1986-08-04
Clearance details
- K-number
- K862751
- Device name
- USA ASPIRATOR
- Applicant
- U. S. A. Medical Corp.
- Decision
- Substantially Equivalent for Some Indications
- Date received
- 1986-07-22
- Decision date
- 1986-08-04
- Days to decision
- 13 days
- Clearance type
- Traditional
- Product code
- BTA
- Device class
- 2
- Regulation number
- 878.4780
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Ogden, UT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.