510(k) K821450

PRESSURE TUBING-ADULT & PEDIATRIC by Gould, Inc. — Product Code DRS

K821450 is an FDA 510(k) premarket notification submitted by Gould, Inc. for the device "PRESSURE TUBING-ADULT & PEDIATRIC". The FDA issued a decision of Substantially Equivalent on May 25, 1982. The device falls under product code DRS (Transducer, Blood-Pressure, Extravascular), a Class II device regulated under 21 CFR 870.2850. Gould, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 25, 1982
Date Received
May 14, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Transducer, Blood-Pressure, Extravascular
Device Class
Class II
Regulation Number
870.2850
Review Panel
CV
Submission Type