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FDA 510(k)

E-20 RAPID CUFF INFLATOR

K-Number: K905367 · 1991-03-06

ApplicantD. E. Hokanson, Inc.
Decision Date1991-03-06
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E-20 RAPID CUFF INFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is D. E. Hokanson, Inc.. It received FDA 510(k) clearance on 1991-03-06 under 510(k) number K905367. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-20 RAPID CUFF INFLATOR?

E-20 RAPID CUFF INFLATOR is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K905367.

When did E-20 RAPID CUFF INFLATOR receive FDA 510(k) clearance?

E-20 RAPID CUFF INFLATOR received FDA 510(k) clearance on 1991-03-06, under 510(k) number K905367.

Who is the listed applicant for E-20 RAPID CUFF INFLATOR?

The FDA 510(k) record lists D. E. Hokanson, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-20 RAPID CUFF INFLATOR?

The FDA product code for E-20 RAPID CUFF INFLATOR is DXN.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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