PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION— 510(k) K911726
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K911726 for PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION, Substantially Equivalent on 1991-10-23. Applicant: Bausch & Lomb, Inc..
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code KHL
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tucker, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.