FDA 510(k)

C-CORD

K-Number: K782046 · 1979-01-10

Decision Date1979-01-10

Product CodeFFZ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

C-CORD is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K782046. The device is classified under product code FFZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-CORD?

C-CORD is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Concept, Inc.. The 510(k) number is K782046.

When did C-CORD receive FDA 510(k) clearance?

C-CORD received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782046.

Who is the listed applicant for C-CORD?

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

What is the FDA product code for C-CORD?

The FDA product code for C-CORD is FFZ.

Other records listing Concept, 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.

K912640CONCEPT ENDOSTEAL FIXATION DEVICE K912957CONCEPT MICROMILL K896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEM K894929STAPLE FIXATION SYSTEM K892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

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Related Devices (Code: FFZ)

K111013ACEMSandhill Scientific, Inc.K822254ELECTRIC CORD FOR ENDOSCOPEKelleher Corp.

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.