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FDA 510(k)

MER BAG

K-Number: K915810 · 1992-03-09

Decision Date1992-03-09
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MER BAG is the device name listed in this FDA 510(k) record. The listed applicant is Merced Medical, Inc.. It received FDA 510(k) clearance on 1992-03-09 under 510(k) number K915810. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MER BAG?

MER BAG is a medical device that received FDA 510(k) clearance on 1992-03-09. The listed applicant is Merced Medical, Inc.. The 510(k) number is K915810.

When did MER BAG receive FDA 510(k) clearance?

MER BAG received FDA 510(k) clearance on 1992-03-09, under 510(k) number K915810.

Who is the listed applicant for MER BAG?

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

What is the FDA product code for MER BAG?

The FDA product code for MER BAG is BTM.

Other records listing Merced 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.

Related Devices (Code: BTM)

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

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

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