510(k) K800946

URINARY CATHETER SAMPLING KIT by Sage Products, Inc. — Product Code KDT

K800946 is an FDA 510(k) premarket notification submitted by Sage Products, Inc. for the device "URINARY CATHETER SAMPLING KIT". The FDA issued a decision of Substantially Equivalent on June 20, 1980. The device falls under product code KDT (Container, Specimen Mailer And Storage, Sterile), a Class I device regulated under 21 CFR 864.3250. Sage Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1980
Date Received
April 22, 1980
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