FDA 510(k)

CONDENSATE COLLECTION KIT

K-Number: K954480 · 1995-12-29

Decision Date1995-12-29

Product CodeCAI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CONDENSATE COLLECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Nova-Ventrx. It received FDA 510(k) clearance on 1995-12-29 under 510(k) number K954480. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDENSATE COLLECTION KIT?

CONDENSATE COLLECTION KIT is a medical device that received FDA 510(k) clearance on 1995-12-29. The listed applicant is Nova-Ventrx. The 510(k) number is K954480.

When did CONDENSATE COLLECTION KIT receive FDA 510(k) clearance?

CONDENSATE COLLECTION KIT received FDA 510(k) clearance on 1995-12-29, under 510(k) number K954480.

Who is the listed applicant for CONDENSATE COLLECTION KIT?

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

What is the FDA product code for CONDENSATE COLLECTION KIT?

The FDA product code for CONDENSATE COLLECTION KIT is CAI.

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Other records listing Nova-Ventrx as applicant

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Related Devices (Code: CAI)

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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.