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FDA 510(k)

PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2

K-Number: K921707 · 1992-07-01

ApplicantPentax Precision Instrument Corp.
Decision Date1992-07-01
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2 is the device name listed in this FDA 510(k) record. The listed applicant is Pentax Precision Instrument Corp.. It received FDA 510(k) clearance on 1992-07-01 under 510(k) number K921707. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2?

PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2 is a medical device that received FDA 510(k) clearance on 1992-07-01. The listed applicant is Pentax Precision Instrument Corp.. The 510(k) number is K921707.

When did PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2 receive FDA 510(k) clearance?

PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2 received FDA 510(k) clearance on 1992-07-01, under 510(k) number K921707.

Who is the listed applicant for PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2?

The FDA 510(k) record lists Pentax Precision Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2?

The FDA product code for PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2 is EOB.

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Other records listing Pentax Precision Instrument Corp. as applicant

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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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