FIBEROPTIC LIGHT SOURCE, FOI-1A— 510(k) K896384
Substantially EquivalentJedmed Instrument Co.
FDA 510(k) clearance K896384 for FIBEROPTIC LIGHT SOURCE, FOI-1A, Substantially Equivalent on 1990-01-23. Applicant: Jedmed Instrument Co.. Device class: 1.
Clearance details
- Applicant
- Jedmed Instrument Co.
- Product code
- Code EQH
- Device class
- Class 1
- Regulation
- 21 CFR 874.4350
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Recent devices under product code EQH
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