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)

IMV FOR MONITORING #M-510

K-Number: K791912 · 1979-10-09

Decision Date1979-10-09
Product CodeCBO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IMV FOR MONITORING #M-510 is the device name listed in this FDA 510(k) record. The listed applicant is Mem Medical, Inc.. It received FDA 510(k) clearance on 1979-10-09 under 510(k) number K791912. The device is classified under product code CBO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMV FOR MONITORING #M-510?

IMV FOR MONITORING #M-510 is a medical device that received FDA 510(k) clearance on 1979-10-09. The listed applicant is Mem Medical, Inc.. The 510(k) number is K791912.

When did IMV FOR MONITORING #M-510 receive FDA 510(k) clearance?

IMV FOR MONITORING #M-510 received FDA 510(k) clearance on 1979-10-09, under 510(k) number K791912.

Who is the listed applicant for IMV FOR MONITORING #M-510?

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

What is the FDA product code for IMV FOR MONITORING #M-510?

The FDA product code for IMV FOR MONITORING #M-510 is CBO.

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 Mem Medical, 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 27 devices →

Related Devices (Code: CBO)

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.

↑