510(k) K923095
K923095 is an FDA 510(k) premarket notification submitted by Kaye Products, Inc. for the device "KAYE MODEL KIAO PELVIC/THIGH STABILIZER". The FDA issued a decision of Substantially Equivalent on July 21, 1992. The device falls under product code INN (Chair, Adjustable, Mechanical), a Class I device regulated under 21 CFR 890.3100. Kaye Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1992
- Date Received
- June 25, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chair, Adjustable, Mechanical
- Device Class
- Class I
- Regulation Number
- 890.3100
- Review Panel
- PM
- Submission Type