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FDA 510(k)

SONICAID MODEL D206E AIR EMBOLI-DETECT

K-Number: K833227 · 1983-10-27

ApplicantSonicaid, Inc.
Decision Date1983-10-27
Product CodeLBA
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

SONICAID MODEL D206E AIR EMBOLI-DETECT is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K833227. The device is classified under product code LBA. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONICAID MODEL D206E AIR EMBOLI-DETECT?

SONICAID MODEL D206E AIR EMBOLI-DETECT is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Sonicaid, Inc.. The 510(k) number is K833227.

When did SONICAID MODEL D206E AIR EMBOLI-DETECT receive FDA 510(k) clearance?

SONICAID MODEL D206E AIR EMBOLI-DETECT received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833227.

Who is the listed applicant for SONICAID MODEL D206E AIR EMBOLI-DETECT?

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

What is the FDA product code for SONICAID MODEL D206E AIR EMBOLI-DETECT?

The FDA product code for SONICAID MODEL D206E AIR EMBOLI-DETECT is LBA.

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Other records listing Sonicaid, Inc. as applicant

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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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