FDA 510(k)

CWD/PPG MODULE

K-Number: K896500 · 1990-07-18

ApplicantLife Sciences Manufacturing, Inc.

Decision Date1990-07-18

Product CodeJOM

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CWD/PPG MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1990-07-18 under 510(k) number K896500. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CWD/PPG MODULE?

CWD/PPG MODULE is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K896500.

When did CWD/PPG MODULE receive FDA 510(k) clearance?

CWD/PPG MODULE received FDA 510(k) clearance on 1990-07-18, under 510(k) number K896500.

Who is the listed applicant for CWD/PPG MODULE?

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

What is the FDA product code for CWD/PPG MODULE?

The FDA product code for CWD/PPG MODULE is JOM.

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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.