510(k) K972126
K972126 is an FDA 510(k) premarket notification submitted by Mednet Locator, Inc. for the device "MYRINGOTOMY TUBE". The FDA issued a decision of Substantially Equivalent on July 29, 1997. The device falls under product code ETD (Tube, Tympanostomy), a Class II device regulated under 21 CFR 874.3880. Mednet Locator, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 1997
- Date Received
- June 5, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Tympanostomy
- Device Class
- Class II
- Regulation Number
- 874.3880
- Review Panel
- EN
- Submission Type