510(k) K872213
K872213 is an FDA 510(k) premarket notification submitted by Medical Wire & Equipment Co. for the device "TRANSTUBE MW176 OT MD176". The FDA issued a decision of Substantially Equivalent on June 23, 1987. The device falls under product code JSM (Culture Media, Non-Propagating Transport), a Class I device regulated under 21 CFR 866.2390. Medical Wire & Equipment Co. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 1987
- Date Received
- June 9, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Non-Propagating Transport
- Device Class
- Class I
- Regulation Number
- 866.2390
- Review Panel
- MI
- Submission Type