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FDA 510(k)

DAVOL LAPAROSCOPIC DISSECTORS

K-Number: K920234 · 1993-02-05

Decision Date1993-02-05
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DAVOL LAPAROSCOPIC DISSECTORS 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 1993-02-05 under 510(k) number K920234. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL LAPAROSCOPIC DISSECTORS?

DAVOL LAPAROSCOPIC DISSECTORS is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K920234.

When did DAVOL LAPAROSCOPIC DISSECTORS receive FDA 510(k) clearance?

DAVOL LAPAROSCOPIC DISSECTORS received FDA 510(k) clearance on 1993-02-05, under 510(k) number K920234.

Who is the listed applicant for DAVOL LAPAROSCOPIC DISSECTORS?

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 DAVOL LAPAROSCOPIC DISSECTORS?

The FDA product code for DAVOL LAPAROSCOPIC DISSECTORS is HET.

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.

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Related Devices (Code: HET)

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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