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FDA 510(k)

PRESSURE LIMITING ELBOW WITH MANOMETER PORT

K-Number: K911298 · 1991-06-25

ApplicantIntertech Resources, Inc.
Decision Date1991-06-25
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRESSURE LIMITING ELBOW WITH MANOMETER PORT is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1991-06-25 under 510(k) number K911298. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE LIMITING ELBOW WITH MANOMETER PORT?

PRESSURE LIMITING ELBOW WITH MANOMETER PORT is a medical device that received FDA 510(k) clearance on 1991-06-25. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K911298.

When did PRESSURE LIMITING ELBOW WITH MANOMETER PORT receive FDA 510(k) clearance?

PRESSURE LIMITING ELBOW WITH MANOMETER PORT received FDA 510(k) clearance on 1991-06-25, under 510(k) number K911298.

Who is the listed applicant for PRESSURE LIMITING ELBOW WITH MANOMETER PORT?

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

What is the FDA product code for PRESSURE LIMITING ELBOW WITH MANOMETER PORT?

The FDA product code for PRESSURE LIMITING ELBOW WITH MANOMETER PORT is BTM.

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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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