510(k) K821723
K821723 is an FDA 510(k) premarket notification submitted by Farrall Instruments, Inc. for the device "BI-4520 DUAL IMPEDOMETER". The FDA issued a decision of Substantially Equivalent on Sep 15, 1982. Farrall Instruments, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 15, 1982
- Date Received
- Jun 9, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No