510(k) K901424

ESOPHAGEAL BALLOON DILATOR by Telemed Systems, Inc. — Product Code KNQ

K901424 is an FDA 510(k) premarket notification submitted by Telemed Systems, Inc. for the device "ESOPHAGEAL BALLOON DILATOR". The FDA issued a decision of Substantially Equivalent on June 21, 1990. The device falls under product code KNQ (Dilator, Esophageal), a Class II device regulated under 21 CFR 876.5365. Telemed Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 21, 1990
Date Received
March 26, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dilator, Esophageal
Device Class
Class II
Regulation Number
876.5365
Review Panel
GU
Submission Type