510(k) K791254

CONPHAR SILICONE DRAINS-STERILE by Conphar, Inc. — Product Code KDQ

K791254 is an FDA 510(k) premarket notification submitted by Conphar, Inc. for the device "CONPHAR SILICONE DRAINS-STERILE". The FDA issued a decision of Substantially Equivalent on Aug 3, 1979. The device falls under product code KDQ (Bottle, Collection, Vacuum), a Class II device regulated under 21 CFR 880.6740. Conphar, Inc. has 121 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Aug 3, 1979
Date Received
Jul 6, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device classification

Device Name
Bottle, Collection, Vacuum
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type
510(k) Exempt

Source: FDA 510(k) database entry for K791254. Report a data issue: hello@regdatalab.com.