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FDA 510(k)

KUMAR CERVICAL APPLICATOR

K-Number: K871213 · 1987-07-16

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date1987-07-16
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KUMAR CERVICAL APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K871213. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KUMAR CERVICAL APPLICATOR?

KUMAR CERVICAL APPLICATOR is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K871213.

When did KUMAR CERVICAL APPLICATOR receive FDA 510(k) clearance?

KUMAR CERVICAL APPLICATOR received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871213.

Who is the listed applicant for KUMAR CERVICAL APPLICATOR?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KUMAR CERVICAL APPLICATOR?

The FDA product code for KUMAR CERVICAL APPLICATOR is IWJ.

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Other records listing Mick Radio-Nuclear Instruments, Inc. as applicant

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Related Devices (Code: IWJ)

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.

K010166IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEMImagyn Medical Technologies, Inc.K980997PGK DEVICE (MODIFIED)Pgk, Inc.K972554REGANES RADIONUCLIDE SEED MAGAZINEAvid N.I.T., Inc.K973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000Avid N.I.T., Inc.K974118WORLDWIDE MEDICAL TECHNOLOGIES SEED IMPLANT NEEDLE SETWorldwide Medical Technologies, LLCK973786NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDENw Radiation Therapy Products

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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