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FDA 510(k)

CANNULA STYLE THERMOCOUPLES

K-Number: K913396 · 1992-05-22

ApplicantPro-Tech, Inc.
Decision Date1992-05-22
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CANNULA STYLE THERMOCOUPLES is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tech, Inc.. It received FDA 510(k) clearance on 1992-05-22 under 510(k) number K913396. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA STYLE THERMOCOUPLES?

CANNULA STYLE THERMOCOUPLES is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Pro-Tech, Inc.. The 510(k) number is K913396.

When did CANNULA STYLE THERMOCOUPLES receive FDA 510(k) clearance?

CANNULA STYLE THERMOCOUPLES received FDA 510(k) clearance on 1992-05-22, under 510(k) number K913396.

Who is the listed applicant for CANNULA STYLE THERMOCOUPLES?

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

What is the FDA product code for CANNULA STYLE THERMOCOUPLES?

The FDA product code for CANNULA STYLE THERMOCOUPLES is BZG.

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Other records listing Pro-Tech, Inc. as applicant

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Related Devices (Code: BZG)

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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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