510(k) K900518

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

K900518 is an FDA 510(k) premarket notification submitted by Helix Medical, Inc. for the device "BLOM-SINGER(R) TRACHEOESOPHAGEAL PUNCTURE KIT". The FDA issued a decision of Substantially Equivalent on June 14, 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
June 14, 1990
Date Received
February 2, 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