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-CONER TM

K-Number: K770641 · 1977-06-24

Decision Date1977-06-24
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINI-CONER TM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Testing System, Inc.. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770641. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI-CONER TM?

MINI-CONER TM is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Medical Testing System, Inc.. The 510(k) number is K770641.

When did MINI-CONER TM receive FDA 510(k) clearance?

MINI-CONER TM received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770641.

Who is the listed applicant for MINI-CONER TM?

The FDA 510(k) record lists Medical Testing System, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI-CONER TM?

The FDA product code for MINI-CONER TM is KNA.

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 Medical Testing System, 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.

Related Devices (Code: KNA)

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.

↑