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FDA 510(k)

VESSEL RETRACTOR, #600732

K-Number: K802244 · 1980-10-03

ApplicantBentley Laboratories, Inc.
Decision Date1980-10-03
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VESSEL RETRACTOR, #600732 is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K802244. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESSEL RETRACTOR, #600732?

VESSEL RETRACTOR, #600732 is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K802244.

When did VESSEL RETRACTOR, #600732 receive FDA 510(k) clearance?

VESSEL RETRACTOR, #600732 received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802244.

Who is the listed applicant for VESSEL RETRACTOR, #600732?

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

What is the FDA product code for VESSEL RETRACTOR, #600732?

The FDA product code for VESSEL RETRACTOR, #600732 is DXC.

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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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