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FDA 510(k)

INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F)

K-Number: K961135 · 1996-04-30

Decision Date1996-04-30
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F) is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1996-04-30 under 510(k) number K961135. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F)?

INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F) is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K961135.

When did INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F) receive FDA 510(k) clearance?

INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F) received FDA 510(k) clearance on 1996-04-30, under 510(k) number K961135.

Who is the listed applicant for INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F)?

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

What is the FDA product code for INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F)?

The FDA product code for INPUT 10F/11/F INTRODUCER SET(010101(10F), 011101(11F) is DYB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 616 devices →

Related Devices (Code: DYB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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