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FDA 510(k)

BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE

K-Number: K924753 · 1992-12-15

Decision Date1992-12-15
Product CodeHMJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE is the device name listed in this FDA 510(k) record. The listed applicant is Bioenterics Corp.. It received FDA 510(k) clearance on 1992-12-15 under 510(k) number K924753. The device is classified under product code HMJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE?

BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE is a medical device that received FDA 510(k) clearance on 1992-12-15. The listed applicant is Bioenterics Corp.. The 510(k) number is K924753.

When did BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE receive FDA 510(k) clearance?

BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE received FDA 510(k) clearance on 1992-12-15, under 510(k) number K924753.

Who is the listed applicant for BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE?

The FDA 510(k) record lists Bioenterics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE?

The FDA product code for BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE is HMJ.

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 Bioenterics Corp. 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: HMJ)

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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