BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT
K-Number: K902112 · 1990-08-01
Advertisement
Device Summary
Frequently Asked Questions
What is the BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT?
BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Helix Medical, Inc.. The 510(k) number is K902112.
When did BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT receive FDA 510(k) clearance?
BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902112.
Who is the listed applicant for BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT?
The FDA 510(k) record lists Helix Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT?
The FDA product code for BLOM-SINGER(R) TRACHEOESOPHAGEAL FISTULA STENT is EWL.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Helix Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EWL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement