510(k) K822252

ENT TREATMENT UNITS by Kelleher Corp. — Product Code ETF

K822252 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "ENT TREATMENT UNITS". The FDA issued a decision of Substantially Equivalent on November 22, 1982. The device falls under product code ETF (Unit, Examining/Treatment, Ent), a Class I device regulated under 21 CFR 874.5300. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 22, 1982
Date Received
July 29, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Examining/Treatment, Ent
Device Class
Class I
Regulation Number
874.5300
Review Panel
EN
Submission Type