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FDA 510(k)

PRESSURE RELIEF VALVE

K-Number: K941492 · 1994-10-26

ApplicantCirculatory Technology, Inc.
Decision Date1994-10-26
Product CodeMNJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE RELIEF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Circulatory Technology, Inc.. It received FDA 510(k) clearance on 1994-10-26 under 510(k) number K941492. The device is classified under product code MNJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE RELIEF VALVE?

PRESSURE RELIEF VALVE is a medical device that received FDA 510(k) clearance on 1994-10-26. The listed applicant is Circulatory Technology, Inc.. The 510(k) number is K941492.

When did PRESSURE RELIEF VALVE receive FDA 510(k) clearance?

PRESSURE RELIEF VALVE received FDA 510(k) clearance on 1994-10-26, under 510(k) number K941492.

Who is the listed applicant for PRESSURE RELIEF VALVE?

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

What is the FDA product code for PRESSURE RELIEF VALVE?

The FDA product code for PRESSURE RELIEF VALVE is MNJ.

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Other records listing Circulatory Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K012942THE V BAG, CATALOG NUMBER VB1800; VAC-BOX FOR VACUUM ASSISTED VENOUS DRAINAGE, CATALOG NUMBER VACBOX1500K001822THE V-BAGK981284BETTER-BLADDER (BB)K964205BETTER-TUBINGK964337BETTER-BLADDER (BB)K961594BETTER-VENTER

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Related Devices (Code: MNJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K992964IBC VENT VALVE, MODEL 1400International Biophysics Corp.

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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