Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MINI MICK APPLICATOR

K-Number: K802032 · 1980-10-23

Decision Date1980-10-23
Product CodeJWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MINI MICK 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 1980-10-23 under 510(k) number K802032. The device is classified under product code JWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI MICK APPLICATOR?

MINI MICK APPLICATOR 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 K802032.

When did MINI MICK APPLICATOR receive FDA 510(k) clearance?

MINI MICK APPLICATOR received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802032.

Who is the listed applicant for MINI MICK 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 MINI MICK APPLICATOR?

The FDA product code for MINI MICK APPLICATOR is JWJ.

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: JWJ)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑