510(k) K822556
K822556 is an FDA 510(k) premarket notification submitted by Bemis Health Care for the device "CRITICAL MEASUREMENT UNIT". The FDA issued a decision of Substantially Equivalent on October 18, 1982. The device falls under product code BYZ (Trap, Sterile Specimen), a Class II device regulated under 21 CFR 880.6740. Bemis Health Care has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 18, 1982
- Date Received
- August 24, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Trap, Sterile Specimen
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type