Upsherscope(Tm)

FDA 510(k) K922275 · Upsher Laryngoscope Co.

Substantially Equivalent

510(k) numberK922275

Submission

Device name
Upsherscope(Tm)
Applicant
Upsher Laryngoscope Co.
Foster City, CA, US
Received
May 14, 1992
Decision date
January 6, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CCW – Laryngoscope, Rigid
Device class
Class I (low risk)
Regulation
21 CFR 868.5540
Specialty
Anesthesiology

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Questions and answers

When was Upsherscope(Tm) cleared by the FDA?

Upsherscope(Tm) (K922275) received a 510(k) decision of Substantially Equivalent on January 6, 1993, 237 days after the submission was received.

What is the product code of K922275?

The FDA product code is CCW – Laryngoscope, Rigid, a Class I (low risk) device regulated under 21 CFR 868.5540.