510(k) K821307
K821307 is an FDA 510(k) premarket notification submitted by Med-Life, Inc. for the device "ANESTHECACHE". The FDA issued a decision of Substantially Equivalent on May 14, 1982. The device falls under product code BRY (Cabinet, Table And Tray, Anesthesia), a Class I device regulated under 21 CFR 868.6100. Med-Life, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 14, 1982
- Date Received
- May 4, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cabinet, Table And Tray, Anesthesia
- Device Class
- Class I
- Regulation Number
- 868.6100
- Review Panel
- AN
- Submission Type