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FDA 510(k)

BOS-CM40,50 HOLDER & RESERVOIR BAG

K-Number: K833670 · 1984-01-03

ApplicantAmerican Bentley
Decision Date1984-01-03
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BOS-CM40,50 HOLDER & RESERVOIR BAG is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833670. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOS-CM40,50 HOLDER & RESERVOIR BAG?

BOS-CM40,50 HOLDER & RESERVOIR BAG is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is American Bentley. The 510(k) number is K833670.

When did BOS-CM40,50 HOLDER & RESERVOIR BAG receive FDA 510(k) clearance?

BOS-CM40,50 HOLDER & RESERVOIR BAG received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833670.

Who is the listed applicant for BOS-CM40,50 HOLDER & RESERVOIR BAG?

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

What is the FDA product code for BOS-CM40,50 HOLDER & RESERVOIR BAG?

The FDA product code for BOS-CM40,50 HOLDER & RESERVOIR BAG is DTZ.

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Related Devices (Code: DTZ)

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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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