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FDA 510(k)

HENSCHKE AFTERLOADING APPLICATOR

K-Number: K871217 · 1987-07-16

Decision Date1987-07-16
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HENSCHKE AFTERLOADING 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 K871217. 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 HENSCHKE AFTERLOADING APPLICATOR?

HENSCHKE AFTERLOADING 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 K871217.

When did HENSCHKE AFTERLOADING APPLICATOR receive FDA 510(k) clearance?

HENSCHKE AFTERLOADING APPLICATOR received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871217.

Who is the listed applicant for HENSCHKE AFTERLOADING 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 HENSCHKE AFTERLOADING APPLICATOR?

The FDA product code for HENSCHKE AFTERLOADING APPLICATOR is IWJ.

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.

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.

View all 42 devices →

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.

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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