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FDA 510(k)

EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO)

K-Number: K883242 · 1988-10-12

ApplicantCancer Technologies, Inc.
Decision Date1988-10-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO) 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 1988-10-12 under 510(k) number K883242. 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 DIMETHYLSULFOXIDE (DMSO)?

EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO) is a medical device that received FDA 510(k) clearance on 1988-10-12. The listed applicant is Cancer Technologies, Inc.. The 510(k) number is K883242.

When did EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO) receive FDA 510(k) clearance?

EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO) received FDA 510(k) clearance on 1988-10-12, under 510(k) number K883242.

Who is the listed applicant for EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO)?

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 DIMETHYLSULFOXIDE (DMSO)?

The FDA product code for EXTRAVAKIT FOR DIMETHYLSULFOXIDE (DMSO) 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.

K883220EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONSK874807EXTRAVAKITK874352TUMORIMETER

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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