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FDA 510(k)

PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION

K-Number: K911726 · 1991-10-23

Decision Date1991-10-23
Product CodeKHL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1991-10-23 under 510(k) number K911726. The device is classified under product code KHL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION?

PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K911726.

When did PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION receive FDA 510(k) clearance?

PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION received FDA 510(k) clearance on 1991-10-23, under 510(k) number K911726.

Who is the listed applicant for PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION?

The FDA product code for PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION is KHL.

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 Bausch & Lomb, 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.

View all 92 devices →

Related Devices (Code: KHL)

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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