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FDA 510(k)

ULTRASONIC AIR-IN-LINE DETECTOR (AILD)

K-Number: K872952 · 1987-10-20

ApplicantImed Corp.
Decision Date1987-10-20
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC AIR-IN-LINE DETECTOR (AILD) is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K872952. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC AIR-IN-LINE DETECTOR (AILD)?

ULTRASONIC AIR-IN-LINE DETECTOR (AILD) is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Imed Corp.. The 510(k) number is K872952.

When did ULTRASONIC AIR-IN-LINE DETECTOR (AILD) receive FDA 510(k) clearance?

ULTRASONIC AIR-IN-LINE DETECTOR (AILD) received FDA 510(k) clearance on 1987-10-20, under 510(k) number K872952.

Who is the listed applicant for ULTRASONIC AIR-IN-LINE DETECTOR (AILD)?

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

What is the FDA product code for ULTRASONIC AIR-IN-LINE DETECTOR (AILD)?

The FDA product code for ULTRASONIC AIR-IN-LINE DETECTOR (AILD) is FRN.

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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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