510(k) K832371
K832371 is an FDA 510(k) premarket notification submitted by Electro-Med Health Industries, Inc. for the device "EGS MODEL 300". The FDA issued a decision of Substantially Equivalent on October 6, 1983. Electro-Med Health Industries, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 1983
- Date Received
- July 18, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No