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FDA 510(k)

UPSHERSCOPE(TM)

K-Number: K922275 · 1993-01-06

ApplicantUpsher Laryngoscope Co.
Decision Date1993-01-06
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UPSHERSCOPE(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Upsher Laryngoscope Co.. It received FDA 510(k) clearance on 1993-01-06 under 510(k) number K922275. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UPSHERSCOPE(TM)?

UPSHERSCOPE(TM) is a medical device that received FDA 510(k) clearance on 1993-01-06. The listed applicant is Upsher Laryngoscope Co.. The 510(k) number is K922275.

When did UPSHERSCOPE(TM) receive FDA 510(k) clearance?

UPSHERSCOPE(TM) received FDA 510(k) clearance on 1993-01-06, under 510(k) number K922275.

Who is the listed applicant for UPSHERSCOPE(TM)?

The FDA 510(k) record lists Upsher Laryngoscope Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UPSHERSCOPE(TM)?

The FDA product code for UPSHERSCOPE(TM) is CCW.

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Related Devices (Code: CCW)

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.

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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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