510(k) K781157
K781157 is an FDA 510(k) premarket notification submitted by Medtech Intl., Inc. for the device "STIMULATOR, NERVE, TRANSCUTANEOUS". The FDA issued a decision of Substantially Equivalent on September 20, 1978. Medtech Intl., Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 20, 1978
- Date Received
- July 5, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No