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FDA 510(k)

T-TUBE WHELAN-MOSS

K-Number: K772292 · 1977-12-20

ApplicantDavol, Inc.
Decision Date1977-12-20
Product CodeGCA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

T-TUBE WHELAN-MOSS is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772292. The device is classified under product code GCA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-TUBE WHELAN-MOSS?

T-TUBE WHELAN-MOSS is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Davol, Inc.. The 510(k) number is K772292.

When did T-TUBE WHELAN-MOSS receive FDA 510(k) clearance?

T-TUBE WHELAN-MOSS received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772292.

Who is the listed applicant for T-TUBE WHELAN-MOSS?

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

What is the FDA product code for T-TUBE WHELAN-MOSS?

The FDA product code for T-TUBE WHELAN-MOSS is GCA.

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Other records listing Davol, Inc. as applicant

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K251557Bard® Mesh; Bard® Mesh Pre-ShapedK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedK031213AQUASENS FLUID MONITORING SYSTEMK030307DAVOL ARTHROVENT OUTFLOW TUBINGK003323COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205K003790DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000, 5552001, 552002, 5552003, 5552004, 5552005

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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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