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FDA 510(k)

MAHURKAR FEMORAL CATHETER

K-Number: K830674 · 1983-05-18

ApplicantQuinton, Inc.
Decision Date1983-05-18
Product CodeLFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAHURKAR FEMORAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K830674. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAHURKAR FEMORAL CATHETER?

MAHURKAR FEMORAL CATHETER is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Quinton, Inc.. The 510(k) number is K830674.

When did MAHURKAR FEMORAL CATHETER receive FDA 510(k) clearance?

MAHURKAR FEMORAL CATHETER received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830674.

Who is the listed applicant for MAHURKAR FEMORAL CATHETER?

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 FEMORAL CATHETER?

The FDA product code for MAHURKAR FEMORAL CATHETER is LFK.

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Other records listing Quinton, 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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, Inc.

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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