Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OXYGENATORS #BOS-10, 105, 5S

K-Number: K823456 · 1982-12-30

Decision Date1982-12-30
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXYGENATORS #BOS-10, 105, 5S 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 1982-12-30 under 510(k) number K823456. 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 OXYGENATORS #BOS-10, 105, 5S?

OXYGENATORS #BOS-10, 105, 5S is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K823456.

When did OXYGENATORS #BOS-10, 105, 5S receive FDA 510(k) clearance?

OXYGENATORS #BOS-10, 105, 5S received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823456.

Who is the listed applicant for OXYGENATORS #BOS-10, 105, 5S?

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 OXYGENATORS #BOS-10, 105, 5S?

The FDA product code for OXYGENATORS #BOS-10, 105, 5S is DTZ.

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 Bentley Laboratories, 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.

View all 55 devices →

Related Devices (Code: DTZ)

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.

↑