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FDA 510(k)

MEDO MEDOMER MBF-100 II

K-Number: K841235 · 1984-11-19

ApplicantMedo U.S.A., Inc.
Decision Date1984-11-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDO MEDOMER MBF-100 II is the device name listed in this FDA 510(k) record. The listed applicant is Medo U.S.A., Inc.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K841235. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDO MEDOMER MBF-100 II?

MEDO MEDOMER MBF-100 II is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Medo U.S.A., Inc.. The 510(k) number is K841235.

When did MEDO MEDOMER MBF-100 II receive FDA 510(k) clearance?

MEDO MEDOMER MBF-100 II received FDA 510(k) clearance on 1984-11-19, under 510(k) number K841235.

Who is the listed applicant for MEDO MEDOMER MBF-100 II?

The FDA 510(k) record lists Medo U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDO MEDOMER MBF-100 II?

The FDA product code for MEDO MEDOMER MBF-100 II is JOW.

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Other records listing Medo U.S.A., 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.

K844064MEDO BUBBLE BATH MA-80, 400, 600 & 700

Related Devices (Code: JOW)

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.

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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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