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FDA 510(k)

SENSOR AMPLIFIER

K-Number: K972515 · 1997-10-02

ApplicantPro-Tech Services, Inc.
Decision Date1997-10-02
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SENSOR AMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tech Services, Inc.. It received FDA 510(k) clearance on 1997-10-02 under 510(k) number K972515. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOR AMPLIFIER?

SENSOR AMPLIFIER is a medical device that received FDA 510(k) clearance on 1997-10-02. The listed applicant is Pro-Tech Services, Inc.. The 510(k) number is K972515.

When did SENSOR AMPLIFIER receive FDA 510(k) clearance?

SENSOR AMPLIFIER received FDA 510(k) clearance on 1997-10-02, under 510(k) number K972515.

Who is the listed applicant for SENSOR AMPLIFIER?

The FDA 510(k) record lists Pro-Tech Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSOR AMPLIFIER?

The FDA product code for SENSOR AMPLIFIER is GWL.

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Other records listing Pro-Tech Services, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GWL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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