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FDA 510(k)

INPUT TUOHY-BORST LOCKING DEVICE

K-Number: K960445 · 1996-08-12

ApplicantC.R. Bard, Inc.
Decision Date1996-08-12
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INPUT TUOHY-BORST LOCKING DEVICE 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 1996-08-12 under 510(k) number K960445. 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 TUOHY-BORST LOCKING DEVICE?

INPUT TUOHY-BORST LOCKING DEVICE is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K960445.

When did INPUT TUOHY-BORST LOCKING DEVICE receive FDA 510(k) clearance?

INPUT TUOHY-BORST LOCKING DEVICE received FDA 510(k) clearance on 1996-08-12, under 510(k) number K960445.

Who is the listed applicant for INPUT TUOHY-BORST LOCKING DEVICE?

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 TUOHY-BORST LOCKING DEVICE?

The FDA product code for INPUT TUOHY-BORST LOCKING DEVICE is DYB.

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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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