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FDA 510(k)

SONICAID MODEL MERIDIAN 800

K-Number: K902690 · 1991-02-05

ApplicantOxford Medilog, Inc.
Decision Date1991-02-05
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SONICAID MODEL MERIDIAN 800 is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1991-02-05 under 510(k) number K902690. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONICAID MODEL MERIDIAN 800?

SONICAID MODEL MERIDIAN 800 is a medical device that received FDA 510(k) clearance on 1991-02-05. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K902690.

When did SONICAID MODEL MERIDIAN 800 receive FDA 510(k) clearance?

SONICAID MODEL MERIDIAN 800 received FDA 510(k) clearance on 1991-02-05, under 510(k) number K902690.

Who is the listed applicant for SONICAID MODEL MERIDIAN 800?

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

What is the FDA product code for SONICAID MODEL MERIDIAN 800?

The FDA product code for SONICAID MODEL MERIDIAN 800 is HGM.

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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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