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FDA 510(k)

PHYSIO-PROBE-HIGH PERMEABILITY CATH.

K-Number: K833433 · 1983-12-29

ApplicantResearch Industries Corp.
Decision Date1983-12-29
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIO-PROBE-HIGH PERMEABILITY CATH. is the device name listed in this FDA 510(k) record. The listed applicant is Research Industries Corp.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833433. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIO-PROBE-HIGH PERMEABILITY CATH.?

PHYSIO-PROBE-HIGH PERMEABILITY CATH. is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Research Industries Corp.. The 510(k) number is K833433.

When did PHYSIO-PROBE-HIGH PERMEABILITY CATH. receive FDA 510(k) clearance?

PHYSIO-PROBE-HIGH PERMEABILITY CATH. received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833433.

Who is the listed applicant for PHYSIO-PROBE-HIGH PERMEABILITY CATH.?

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

What is the FDA product code for PHYSIO-PROBE-HIGH PERMEABILITY CATH.?

The FDA product code for PHYSIO-PROBE-HIGH PERMEABILITY CATH. is DQY.

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Other records listing Research Industries Corp. 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.

K945931RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVEK832542I.V. ADMINISTRATION SETK831769VARIOUS CARDIOVASCULAR SURGICAL DEVICEK831759INTRACARDIA SUCKERS

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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