510(k) K800233

ABCO MIDSTREAM URINE COLLECTION SET by Abco Dealers, Inc. — Product Code FMH

K800233 is an FDA 510(k) premarket notification submitted by Abco Dealers, Inc. for the device "ABCO MIDSTREAM URINE COLLECTION SET". The FDA issued a decision of Substantially Equivalent on February 26, 1980. The device falls under product code FMH (Container, Specimen, Sterile), a Class I device regulated under 21 CFR 864.3250. Abco Dealers, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1980
Date Received
February 5, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Container, Specimen, Sterile
Device Class
Class I
Regulation Number
864.3250
Review Panel
HO
Submission Type