PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2— 510(k) K921707

Substantially Equivalent

Pentax Precision Instrument Corp.

FDA 510(k) clearance K921707 for PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2, Substantially Equivalent on 1992-07-01. Applicant: Pentax Precision Instrument Corp..

Clearance details

Applicant: Pentax Precision Instrument Corp.
Product code: Code EOB
Advisory panel: Ear, Nose, Throat
Date received: 1992-04-10
Decision date: 1992-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

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Adverse events under product code EOB

product code EOB

Malfunction: 6,143
Total: 6,143

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.