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FDA 510(k)

THORASTAT ATR-XXXX

K-Number: K870792 · 1987-04-28

ApplicantGish Biomedical, Inc.
Decision Date1987-04-28
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THORASTAT ATR-XXXX is the device name listed in this FDA 510(k) record. The listed applicant is Gish Biomedical, Inc.. It received FDA 510(k) clearance on 1987-04-28 under 510(k) number K870792. The device is classified under product code DTP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORASTAT ATR-XXXX?

THORASTAT ATR-XXXX is a medical device that received FDA 510(k) clearance on 1987-04-28. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K870792.

When did THORASTAT ATR-XXXX receive FDA 510(k) clearance?

THORASTAT ATR-XXXX received FDA 510(k) clearance on 1987-04-28, under 510(k) number K870792.

Who is the listed applicant for THORASTAT ATR-XXXX?

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

What is the FDA product code for THORASTAT ATR-XXXX?

The FDA product code for THORASTAT ATR-XXXX is DTP.

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Other records listing Gish Biomedical, 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.

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