Clearance Summary
ASPIRATING ENDO OCULAR PROBE received FDA 510(k) clearance under submission number K930123, sponsored by Surgical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1994-02-16.
- Submission: K930123
- Applicant / Sponsor: Surgical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4350
- Decision date: 1994-02-16
Classification & Regulation
This clearance is catalogued under FDA product code EQH and 21 CFR 874.4350, within the Ear, Nose, Throat review panel as a Class I device.