510(k) K931462
K931462 is an FDA 510(k) premarket notification submitted by Glenroe Technologies, Inc. for the device "GLENROE CHAIN". The FDA issued a decision of Substantially Equivalent on July 22, 1993. The device falls under product code ECI (Band, Elastic, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Glenroe Technologies, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 22, 1993
- Date Received
- March 24, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Band, Elastic, Orthodontic
- Device Class
- Class I
- Regulation Number
- 872.5410
- Review Panel
- DE
- Submission Type