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FDA 510(k)

QUICK SEEDER

K-Number: K913293 · 1992-10-13

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date1992-10-13
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QUICK SEEDER 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 1992-10-13 under 510(k) number K913293. 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 QUICK SEEDER?

QUICK SEEDER is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K913293.

When did QUICK SEEDER receive FDA 510(k) clearance?

QUICK SEEDER received FDA 510(k) clearance on 1992-10-13, under 510(k) number K913293.

Who is the listed applicant for QUICK SEEDER?

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 QUICK SEEDER?

The FDA product code for QUICK SEEDER 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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