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FDA 510(k)

HEMODIALYSIS CANNULA & FEMORAL CLAMP

K-Number: K760973 · 1977-01-12

ApplicantRodell Medical, Inc.
Decision Date1977-01-12
Product CodeFIQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMODIALYSIS CANNULA & FEMORAL CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Rodell Medical, Inc.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K760973. The device is classified under product code FIQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMODIALYSIS CANNULA & FEMORAL CLAMP?

HEMODIALYSIS CANNULA & FEMORAL CLAMP is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Rodell Medical, Inc.. The 510(k) number is K760973.

When did HEMODIALYSIS CANNULA & FEMORAL CLAMP receive FDA 510(k) clearance?

HEMODIALYSIS CANNULA & FEMORAL CLAMP received FDA 510(k) clearance on 1977-01-12, under 510(k) number K760973.

Who is the listed applicant for HEMODIALYSIS CANNULA & FEMORAL CLAMP?

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

What is the FDA product code for HEMODIALYSIS CANNULA & FEMORAL CLAMP?

The FDA product code for HEMODIALYSIS CANNULA & FEMORAL CLAMP is FIQ.

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Related Devices (Code: FIQ)

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.

K892887ST SERIES SAF-T-SHUNTS ARTERIOVENOUS CANNULAAkcess Medical Products, Inc.K892666SAF-T-SHUNT, S-300 SERIESAkcess Medical Products, Inc.K892663S-100 ALLEN-BROWN SHUNTAkcess Medical Products, Inc.K844692PEDIATRIC SIZED HEMOCATH CATHETERQuinton, Inc.K841791PLUME FISTULA NEEDLEHospal Medical Corp.K840322HEMOFILTRATION CATHETER HF-100Vas-Cath of Canada , Ltd.

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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