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FDA 510(k)

BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET

K-Number: K920090 · 1992-09-10

Decision Date1992-09-10
Product CodeEWL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET is the device name listed in this FDA 510(k) record. The listed applicant is Helix Medical, Inc.. It received FDA 510(k) clearance on 1992-09-10 under 510(k) number K920090. The device is classified under product code EWL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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