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FDA 510(k)

ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES

K-Number: K911884 · 1994-07-05

ApplicantAdvance Medical Designs, Inc.
Decision Date1994-07-05
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1994-07-05 under 510(k) number K911884. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES?

ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES is a medical device that received FDA 510(k) clearance on 1994-07-05. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K911884.

When did ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES receive FDA 510(k) clearance?

ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES received FDA 510(k) clearance on 1994-07-05, under 510(k) number K911884.

Who is the listed applicant for ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES?

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

What is the FDA product code for ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES?

The FDA product code for ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES is DTL.

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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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