510(k) K902112
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