FDA 510(k)

SAVE MOR

K-Number: K801945 · 1980-11-19

Decision Date1980-11-19

Product CodeDRM

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SAVE MOR is the device name listed in this FDA 510(k) record. The listed applicant is Cardia Concepts Corp.. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K801945. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAVE MOR?

SAVE MOR is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Cardia Concepts Corp.. The 510(k) number is K801945.

When did SAVE MOR receive FDA 510(k) clearance?

SAVE MOR received FDA 510(k) clearance on 1980-11-19, under 510(k) number K801945.

Who is the listed applicant for SAVE MOR?

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

What is the FDA product code for SAVE MOR?

The FDA product code for SAVE MOR is DRM.

Other records listing Cardia Concepts Corp. 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.

K801947CPR TRAVELER K801946CPR HELPER

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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.