FDA 510(k)

IPG-II MODULE

K-Number: K903700 · 1991-01-16

ApplicantLife Sciences Manufacturing, Inc.

Decision Date1991-01-16

Product CodeDSB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

IPG-II 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 1991-01-16 under 510(k) number K903700. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPG-II MODULE?

IPG-II MODULE is a medical device that received FDA 510(k) clearance on 1991-01-16. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K903700.

When did IPG-II MODULE receive FDA 510(k) clearance?

IPG-II MODULE received FDA 510(k) clearance on 1991-01-16, under 510(k) number K903700.

Who is the listed applicant for IPG-II 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 IPG-II MODULE?

The FDA product code for IPG-II MODULE is DSB.

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Other records listing Life Sciences Manufacturing, 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.