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FDA 510(k)

PRESSURE RELIEF ADAPTOR

K-Number: K850559 · 1985-04-25

ApplicantPrecision Medical, Inc.
Decision Date1985-04-25
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRESSURE RELIEF ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K850559. The device is classified under product code CAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE RELIEF ADAPTOR?

PRESSURE RELIEF ADAPTOR is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Precision Medical, Inc.. The 510(k) number is K850559.

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

PRESSURE RELIEF ADAPTOR received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850559.

Who is the listed applicant for PRESSURE RELIEF ADAPTOR?

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

What is the FDA product code for PRESSURE RELIEF ADAPTOR?

The FDA product code for PRESSURE RELIEF ADAPTOR is CAX.

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Related Devices (Code: CAX)

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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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