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FDA 510(k)

RADIOASSAY, CONCEPT 4

K-Number: K760006 · 1976-07-20

ApplicantMicromedic Systems
Decision Date1976-07-20
Product Code
DecisionSubstantially Equivalent

Device Summary

RADIOASSAY, CONCEPT 4 is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760006. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOASSAY, CONCEPT 4?

RADIOASSAY, CONCEPT 4 is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Micromedic Systems. The 510(k) number is K760006.

When did RADIOASSAY, CONCEPT 4 receive FDA 510(k) clearance?

RADIOASSAY, CONCEPT 4 received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760006.

Who is the listed applicant for RADIOASSAY, CONCEPT 4?

The FDA 510(k) record lists Micromedic Systems as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Micromedic Systems 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.

K923643MEDICOOLK872309MICROMEDIC COMBOSTAT LH/FSH KITK871505AUTOPAK NEONATAL TSH MONOCLONAL IRMA KITK870904MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KITK871008MICROMEDIC NEONATAL T4 KITK870245AUTOPAK TSH MONOCLONAL IRMA KIT

View all 42 devices →

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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