510(k) K936200
K936200 is an FDA 510(k) premarket notification submitted by Canon USA, Inc. for the device "WIRELESS CHART PROJECTOR,HCP-W 721". The FDA issued a decision of Substantially Equivalent on September 28, 1994. The device falls under product code HOS (Projector, Ophthalmic), a Class I device regulated under 21 CFR 886.1680. Canon USA, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 28, 1994
- Date Received
- December 29, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Projector, Ophthalmic
- Device Class
- Class I
- Regulation Number
- 886.1680
- Review Panel
- OP
- Submission Type