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FDA 510(k)

SONICAID MODEL VASOFLO 4

K-Number: K895909 · 1990-07-09

ApplicantOxford Medilog, Inc.
Decision Date1990-07-09
Product CodeMAA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SONICAID MODEL VASOFLO 4 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 1990-07-09 under 510(k) number K895909. The device is classified under product code MAA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONICAID MODEL VASOFLO 4?

SONICAID MODEL VASOFLO 4 is a medical device that received FDA 510(k) clearance on 1990-07-09. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K895909.

When did SONICAID MODEL VASOFLO 4 receive FDA 510(k) clearance?

SONICAID MODEL VASOFLO 4 received FDA 510(k) clearance on 1990-07-09, under 510(k) number K895909.

Who is the listed applicant for SONICAID MODEL VASOFLO 4?

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 VASOFLO 4?

The FDA product code for SONICAID MODEL VASOFLO 4 is MAA.

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Other records listing Oxford Medilog, Inc. as applicant

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Related Devices (Code: MAA)

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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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