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FDA 510(k)

FOUR-CHANNEL PREAMPLIFIER

K-Number: K962455 · 1997-01-13

ApplicantCadwell Laboratories, Inc.
Decision Date1997-01-13
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FOUR-CHANNEL PREAMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1997-01-13 under 510(k) number K962455. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOUR-CHANNEL PREAMPLIFIER?

FOUR-CHANNEL PREAMPLIFIER is a medical device that received FDA 510(k) clearance on 1997-01-13. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K962455.

When did FOUR-CHANNEL PREAMPLIFIER receive FDA 510(k) clearance?

FOUR-CHANNEL PREAMPLIFIER received FDA 510(k) clearance on 1997-01-13, under 510(k) number K962455.

Who is the listed applicant for FOUR-CHANNEL PREAMPLIFIER?

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

What is the FDA product code for FOUR-CHANNEL PREAMPLIFIER?

The FDA product code for FOUR-CHANNEL PREAMPLIFIER is GWF.

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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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