510(k) K771056
K771056 is an FDA 510(k) premarket notification submitted by Sherwood Medical Industries for the device "BLOOD COLLECTION TUBE, GREEN". The FDA issued a decision of Substantially Equivalent on June 29, 1977. The device falls under product code GIM (Tubes, Vacuum Sample, With Anticoagulant), a Class II device regulated under 21 CFR 862.1675. Sherwood Medical Industries has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 29, 1977
- Date Received
- June 13, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubes, Vacuum Sample, With Anticoagulant
- Device Class
- Class II
- Regulation Number
- 862.1675
- Review Panel
- CH
- Submission Type