Clearance Summary
910T MONTORIZED INSTRUMENT TABLE received FDA 510(k) clearance under submission number K922242, sponsored by R.H. Burton Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1992-09-30.
- Submission: K922242
- Applicant / Sponsor: R.H. Burton Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4855
- Decision date: 1992-09-30
Classification & Regulation
This clearance is catalogued under FDA product code HRJ and 21 CFR 886.4855, within the Ophthalmic review panel as a Class I device.