510(k) K781400

HEMOVAC TUBING MATERIAL CHANGE by Snyder Laboratories, Inc. — Product Code GCY

K781400 is an FDA 510(k) premarket notification submitted by Snyder Laboratories, Inc. for the device "HEMOVAC TUBING MATERIAL CHANGE". The FDA issued a decision of Substantially Equivalent on September 20, 1978. The device falls under product code GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered), a Class I device regulated under 21 CFR 878.4680. Snyder Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 20, 1978
Date Received
August 15, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Device Class
Class I
Regulation Number
878.4680
Review Panel
SU
Submission Type