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FDA 510(k)

NEOGUARD CHEST PERCUSSOR

K-Number: K853965 · 1985-12-03

ApplicantCas Medical Systems, Inc.
Decision Date1985-12-03
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOGUARD CHEST PERCUSSOR is the device name listed in this FDA 510(k) record. The listed applicant is Cas Medical Systems, Inc.. It received FDA 510(k) clearance on 1985-12-03 under 510(k) number K853965. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOGUARD CHEST PERCUSSOR?

NEOGUARD CHEST PERCUSSOR is a medical device that received FDA 510(k) clearance on 1985-12-03. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K853965.

When did NEOGUARD CHEST PERCUSSOR receive FDA 510(k) clearance?

NEOGUARD CHEST PERCUSSOR received FDA 510(k) clearance on 1985-12-03, under 510(k) number K853965.

Who is the listed applicant for NEOGUARD CHEST PERCUSSOR?

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

What is the FDA product code for NEOGUARD CHEST PERCUSSOR?

The FDA product code for NEOGUARD CHEST PERCUSSOR is BYI.

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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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