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FDA 510(k)

PALEY TRANSPARENT MANIFOLD

K-Number: K760843 · 1976-11-12

ApplicantUsci, Div. C.R. Bard, Inc.
Decision Date1976-11-12
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PALEY TRANSPARENT MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Usci, Div. C.R. Bard, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760843. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALEY TRANSPARENT MANIFOLD?

PALEY TRANSPARENT MANIFOLD is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Usci, Div. C.R. Bard, Inc.. The 510(k) number is K760843.

When did PALEY TRANSPARENT MANIFOLD receive FDA 510(k) clearance?

PALEY TRANSPARENT MANIFOLD received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760843.

Who is the listed applicant for PALEY TRANSPARENT MANIFOLD?

The FDA 510(k) record lists Usci, Div. C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALEY TRANSPARENT MANIFOLD?

The FDA product code for PALEY TRANSPARENT MANIFOLD is DTL.

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Other records listing Usci, Div. C.R. Bard, Inc. as applicant

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K940092USCI INPUT INTRODUCER SETK884209USCI DORROS INFUSION/PROBING CATHETERK771823CATHETER, CARDIOVASCULARK771982888 ARTERIAL/VENOUS CATHETER INTRODUCERK772021TRC STAINLESS STEEL SAFETY SPRING GUIDESK770835PATCH FABRIC

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Related Devices (Code: DTL)

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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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