510(k) K922150
K922150 is an FDA 510(k) premarket notification submitted by Air-Shields, Inc. for the device "EXAMINATION LAMP". The FDA issued a decision of Substantially Equivalent on July 21, 1992. The device falls under product code KZF (Device, Medical Examination, Ac Powered), a Class I device regulated under 21 CFR 880.6320. Air-Shields, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1992
- Date Received
- May 7, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Medical Examination, Ac Powered
- Device Class
- Class I
- Regulation Number
- 880.6320
- Review Panel
- HO
- Submission Type