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FDA 510(k)

EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS

K-Number: K883220 · 1988-10-20

ApplicantCancer Technologies, Inc.
Decision Date1988-10-20
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Cancer Technologies, Inc.. It received FDA 510(k) clearance on 1988-10-20 under 510(k) number K883220. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS?

EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS is a medical device that received FDA 510(k) clearance on 1988-10-20. The listed applicant is Cancer Technologies, Inc.. The 510(k) number is K883220.

When did EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS receive FDA 510(k) clearance?

EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS received FDA 510(k) clearance on 1988-10-20, under 510(k) number K883220.

Who is the listed applicant for EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS?

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

What is the FDA product code for EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS?

The FDA product code for EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS is FMF.

Related Clinical Trials

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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Other records listing Cancer Technologies, 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.

K883242EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO)K874807EXTRAVAKITK874352TUMORIMETER

Related Devices (Code: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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