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FDA 510(k)

USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR

K-Number: K884104 · 1988-12-21

ApplicantC.R. Bard, Inc.
Decision Date1988-12-21
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR 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 1988-12-21 under 510(k) number K884104. 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 USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR?

USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR is a medical device that received FDA 510(k) clearance on 1988-12-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K884104.

When did USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR receive FDA 510(k) clearance?

USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR received FDA 510(k) clearance on 1988-12-21, under 510(k) number K884104.

Who is the listed applicant for USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR?

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 USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR?

The FDA product code for USCI(R) HEMAQUET(TM) INTRODUCER W/OBTURATOR 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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