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FDA 510(k)

AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P

K-Number: K983631 · 1999-07-01

ApplicantInstrumentation Industries, Inc.
Decision Date1999-07-01
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1999-07-01 under 510(k) number K983631. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P?

AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K983631.

When did AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P receive FDA 510(k) clearance?

AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P received FDA 510(k) clearance on 1999-07-01, under 510(k) number K983631.

Who is the listed applicant for AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P?

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

What is the FDA product code for AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P?

The FDA product code for AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P is CBP.

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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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