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FDA 510(k)

MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT

K-Number: K852388 · 1985-08-22

ApplicantQuinton, Inc.
Decision Date1985-08-22
Product CodeDQY
Advisory CommitteeCV
DecisionUnknown

Device Summary

MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1985-08-22 under 510(k) number K852388. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT?

MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT is a medical device that received FDA 510(k) clearance on 1985-08-22. The listed applicant is Quinton, Inc.. The 510(k) number is K852388.

When did MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT receive FDA 510(k) clearance?

MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT received FDA 510(k) clearance on 1985-08-22, under 510(k) number K852388.

Who is the listed applicant for MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT?

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

What is the FDA product code for MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT?

The FDA product code for MAHURKAR SUBCLAVIAN CATHETER INSERTION KIT is DQY.

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Other records listing Quinton, Inc. as applicant

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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.

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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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