510(k) K833660

PRESERV PVA FIXATIVE -MALIN PACK by Preventive Diagnostics Corp. — Product Code KDT

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