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FDA 510(k)

STRYKER PRESSURE SENSING CANNULA

K-Number: K944593 · 1995-09-01

ApplicantStryker Endoscopy
Decision Date1995-09-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER PRESSURE SENSING CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K944593. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PRESSURE SENSING CANNULA?

STRYKER PRESSURE SENSING CANNULA is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Stryker Endoscopy. The 510(k) number is K944593.

When did STRYKER PRESSURE SENSING CANNULA receive FDA 510(k) clearance?

STRYKER PRESSURE SENSING CANNULA received FDA 510(k) clearance on 1995-09-01, under 510(k) number K944593.

Who is the listed applicant for STRYKER PRESSURE SENSING CANNULA?

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

What is the FDA product code for STRYKER PRESSURE SENSING CANNULA?

The FDA product code for STRYKER PRESSURE SENSING CANNULA is HRX.

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Related Devices (Code: HRX)

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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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