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FDA 510(k)

MOD. MCI 17 MANUAL CUFF INFLATOR

K-Number: K800767 · 1980-04-24

ApplicantMedasonics, Inc.
Decision Date1980-04-24
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOD. MCI 17 MANUAL CUFF INFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1980-04-24 under 510(k) number K800767. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOD. MCI 17 MANUAL CUFF INFLATOR?

MOD. MCI 17 MANUAL CUFF INFLATOR is a medical device that received FDA 510(k) clearance on 1980-04-24. The listed applicant is Medasonics, Inc.. The 510(k) number is K800767.

When did MOD. MCI 17 MANUAL CUFF INFLATOR receive FDA 510(k) clearance?

MOD. MCI 17 MANUAL CUFF INFLATOR received FDA 510(k) clearance on 1980-04-24, under 510(k) number K800767.

Who is the listed applicant for MOD. MCI 17 MANUAL CUFF INFLATOR?

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

What is the FDA product code for MOD. MCI 17 MANUAL CUFF INFLATOR?

The FDA product code for MOD. MCI 17 MANUAL CUFF INFLATOR is DXQ.

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Related Devices (Code: DXQ)

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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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