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FDA 510(k)

RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT

K-Number: K821480 · 1982-06-17

ApplicantThe Healthcare Group Laboratories, Inc.
Decision Date1982-06-17
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1982-06-17 under 510(k) number K821480. 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 RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT?

RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT is a medical device that received FDA 510(k) clearance on 1982-06-17. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K821480.

When did RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT receive FDA 510(k) clearance?

RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT received FDA 510(k) clearance on 1982-06-17, under 510(k) number K821480.

Who is the listed applicant for RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT?

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

What is the FDA product code for RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT?

The FDA product code for RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT is DQY.

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Other records listing The Healthcare Group Laboratories, 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.

K850035EMPTY SOLUTION TRANSFER CONTAINERK842170EMPTY SOLUTION TRANSFER CONTAINERK842091DISPOS. ACU-CUT SOFT TISSUE BIOPSYK840742RIGHT ATRIAL CATHETERK830299SOLUTION TRANSFER CONTAINERK822307ADHESIVE SPRAY #4050-4060

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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

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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