PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION
K-Number: K911726 · 1991-10-23
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement