FDA 510(k)

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

K-Number: K900314 · 1990-10-26

Decision Date1990-10-26

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent for Some Indications

Device Summary

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN is the device name listed in this FDA 510(k) record. The listed applicant is Percussionaire Corp.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K900314. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN?

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Percussionaire Corp.. The 510(k) number is K900314.

When did PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN receive FDA 510(k) clearance?

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN received FDA 510(k) clearance on 1990-10-26, under 510(k) number K900314.

Who is the listed applicant for PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN?

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

What is the FDA product code for PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN?

The FDA product code for PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN is CBK.

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Other records listing Percussionaire Corp. 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.