510(k) K960401

ULTIMATE SEAL by Hans Rudolph, Inc. — Product Code KGB

K960401 is an FDA 510(k) premarket notification submitted by Hans Rudolph, Inc. for the device "ULTIMATE SEAL". The FDA issued a decision of Substantially Equivalent on June 20, 1996. The device falls under product code KGB (Mask, Oxygen, Non-Rebreathing), a Class I device regulated under 21 CFR 868.5570. Hans Rudolph, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1996
Date Received
January 29, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mask, Oxygen, Non-Rebreathing
Device Class
Class I
Regulation Number
868.5570
Review Panel
AN
Submission Type