510(k) K802691
K802691 is an FDA 510(k) premarket notification submitted by Occumedics, Inc. for the device "OCCUPAK CAT.#200-0538". The FDA issued a decision of SESP on October 27, 1980. Occumedics, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESP ()
- Decision Date
- October 27, 1980
- Date Received
- October 27, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No