TISSUE SECTION ADHESIVE
FDA 510(k) clearance K881659 · decided 1988-04-21
Clearance details
- K-number
- K881659
- Device name
- TISSUE SECTION ADHESIVE
- Applicant
- Surgipath Medical Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-15
- Decision date
- 1988-04-21
- Days to decision
- 6 days
- Clearance type
- Traditional
- Product code
- IFZ
- Device class
- 1
- Regulation number
- 864.4010
- Medical specialty
- Pathology
- Advisory committee
- Pathology
- Location
- Grayslake, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.