510(k) K833660
K833660 is an FDA 510(k) premarket notification submitted by Preventive Diagnostics Corp. for the device "PRESERV PVA FIXATIVE -MALIN PACK". The FDA issued a decision of Substantially Equivalent on November 28, 1983. The device falls under product code KDT (Container, Specimen Mailer And Storage, Sterile), a Class I device regulated under 21 CFR 864.3250. Preventive Diagnostics Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 28, 1983
- Date Received
- October 18, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Container, Specimen Mailer And Storage, Sterile
- Device Class
- Class I
- Regulation Number
- 864.3250
- Review Panel
- PA
- Submission Type