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)

CAVENDISH 460/680 ANESTHESIA MACHINE

K-Number: K884802 · 1989-08-01

Decision Date1989-08-01
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAVENDISH 460/680 ANESTHESIA MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1989-08-01 under 510(k) number K884802. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAVENDISH 460/680 ANESTHESIA MACHINE?

CAVENDISH 460/680 ANESTHESIA MACHINE is a medical device that received FDA 510(k) clearance on 1989-08-01. The listed applicant is Dentsply Intl.. The 510(k) number is K884802.

When did CAVENDISH 460/680 ANESTHESIA MACHINE receive FDA 510(k) clearance?

CAVENDISH 460/680 ANESTHESIA MACHINE received FDA 510(k) clearance on 1989-08-01, under 510(k) number K884802.

Who is the listed applicant for CAVENDISH 460/680 ANESTHESIA MACHINE?

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

What is the FDA product code for CAVENDISH 460/680 ANESTHESIA MACHINE?

The FDA product code for CAVENDISH 460/680 ANESTHESIA MACHINE is BSZ.

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 Dentsply Intl. 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 279 devices →

Related Devices (Code: BSZ)

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.

↑