BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET
K-Number: K920090 · 1992-09-10
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Device Summary
Frequently Asked Questions
What is the BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET?
BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET is a medical device that received FDA 510(k) clearance on 1992-09-10. The listed applicant is Helix Medical, Inc.. The 510(k) number is K920090.
When did BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET receive FDA 510(k) clearance?
BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET received FDA 510(k) clearance on 1992-09-10, under 510(k) number K920090.
Who is the listed applicant for BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET?
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 TRACHEOESOPHAGEAL PUNCTURE SET?
The FDA product code for BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET 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.
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