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FDA 510(k)

MULTI-LUMEN INTRAVENOUS INFUSION CATH

K-Number: K833825 · 1984-01-10

ApplicantMedical Parameters, Inc.
Decision Date1984-01-10
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTI-LUMEN INTRAVENOUS INFUSION CATH is the device name listed in this FDA 510(k) record. The listed applicant is Medical Parameters, Inc.. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K833825. 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 MULTI-LUMEN INTRAVENOUS INFUSION CATH?

MULTI-LUMEN INTRAVENOUS INFUSION CATH is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Medical Parameters, Inc.. The 510(k) number is K833825.

When did MULTI-LUMEN INTRAVENOUS INFUSION CATH receive FDA 510(k) clearance?

MULTI-LUMEN INTRAVENOUS INFUSION CATH received FDA 510(k) clearance on 1984-01-10, under 510(k) number K833825.

Who is the listed applicant for MULTI-LUMEN INTRAVENOUS INFUSION CATH?

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

What is the FDA product code for MULTI-LUMEN INTRAVENOUS INFUSION CATH?

The FDA product code for MULTI-LUMEN INTRAVENOUS INFUSION CATH is DQY.

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Other records listing Medical Parameters, 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.

K862190WALRUS: DOUBLE BALLOON SHUNTING CATHETERK844444ESOPHAGEAL STETHOSCOPEK830754BLOOD PRESSURE MONITORING KITS,WALRUSK831239WALRUS PERCUTANEOUS INTRODUCER SETK830755I.V. SETS WALRUS BRAND VARIOUS CONFIGUR-

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.

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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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