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FDA 510(k)

PRESSURE GAUGE ACCESSORY KIT/DILATATION

K-Number: K802261 · 1980-10-03

ApplicantStanco Medical, Inc.
Decision Date1980-10-03
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE GAUGE ACCESSORY KIT/DILATATION 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 1980-10-03 under 510(k) number K802261. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE GAUGE ACCESSORY KIT/DILATATION?

PRESSURE GAUGE ACCESSORY KIT/DILATATION is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Stanco Medical, Inc.. The 510(k) number is K802261.

When did PRESSURE GAUGE ACCESSORY KIT/DILATATION receive FDA 510(k) clearance?

PRESSURE GAUGE ACCESSORY KIT/DILATATION received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802261.

Who is the listed applicant for PRESSURE GAUGE ACCESSORY KIT/DILATATION?

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 PRESSURE GAUGE ACCESSORY KIT/DILATATION?

The FDA product code for PRESSURE GAUGE ACCESSORY KIT/DILATATION is DWF.

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Other records listing Stanco Medical, Inc. as applicant

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Related Devices (Code: DWF)

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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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