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FDA 510(k)

SCOTT NEEDLE & SCOTT MICK IMPLANTER

K-Number: K801983 · 1980-10-23

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date1980-10-23
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCOTT NEEDLE & SCOTT MICK IMPLANTER 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 1980-10-23 under 510(k) number K801983. 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 SCOTT NEEDLE & SCOTT MICK IMPLANTER?

SCOTT NEEDLE & SCOTT MICK IMPLANTER is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K801983.

When did SCOTT NEEDLE & SCOTT MICK IMPLANTER receive FDA 510(k) clearance?

SCOTT NEEDLE & SCOTT MICK IMPLANTER received FDA 510(k) clearance on 1980-10-23, under 510(k) number K801983.

Who is the listed applicant for SCOTT NEEDLE & SCOTT MICK IMPLANTER?

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 SCOTT NEEDLE & SCOTT MICK IMPLANTER?

The FDA product code for SCOTT NEEDLE & SCOTT MICK IMPLANTER is IWJ.

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Other records listing Mick Radio-Nuclear Instruments, 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.

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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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