510(k) K902112

BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT by Helix Medical, Inc. — Product Code EWL

K902112 is an FDA 510(k) premarket notification submitted by Helix Medical, Inc. for the device "BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT". The FDA issued a decision of Substantially Equivalent on August 1, 1990. The device falls under product code EWL (Prosthesis, Laryngeal (Taub)), a Class II device regulated under 21 CFR 874.3730. Helix Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 1990
Date Received
May 9, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Laryngeal (Taub)
Device Class
Class II
Regulation Number
874.3730
Review Panel
EN
Submission Type