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FDA 510(k)

DISP. TOUGY-BORST TYPE ADAPTOR W/PORT

K-Number: K802328 · 1980-10-10

ApplicantStanco Medical, Inc.
Decision Date1980-10-10
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISP. TOUGY-BORST TYPE ADAPTOR W/PORT is the device name listed in this FDA 510(k) record. The listed applicant is Stanco Medical, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802328. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISP. TOUGY-BORST TYPE ADAPTOR W/PORT?

DISP. TOUGY-BORST TYPE ADAPTOR W/PORT is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Stanco Medical, Inc.. The 510(k) number is K802328.

When did DISP. TOUGY-BORST TYPE ADAPTOR W/PORT receive FDA 510(k) clearance?

DISP. TOUGY-BORST TYPE ADAPTOR W/PORT received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802328.

Who is the listed applicant for DISP. TOUGY-BORST TYPE ADAPTOR W/PORT?

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

What is the FDA product code for DISP. TOUGY-BORST TYPE ADAPTOR W/PORT?

The FDA product code for DISP. TOUGY-BORST TYPE ADAPTOR W/PORT is DTZ.

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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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