Clearance Summary
ARTHROSCOPE received FDA 510(k) clearance under submission number K931792, sponsored by Intramed Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-06-13.
- Submission: K931792
- Applicant / Sponsor: Intramed Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4350
- Decision date: 1994-06-13
Classification & Regulation
This clearance is catalogued under FDA product code HRH and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.