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FDA 510(k)

ADULT VENTILATOR TESTER VT-1

K-Number: K853760 · 1985-12-03

Decision Date1985-12-03
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ADULT VENTILATOR TESTER VT-1 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tek Instruments, Inc.. It received FDA 510(k) clearance on 1985-12-03 under 510(k) number K853760. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT VENTILATOR TESTER VT-1?

ADULT VENTILATOR TESTER VT-1 is a medical device that received FDA 510(k) clearance on 1985-12-03. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K853760.

When did ADULT VENTILATOR TESTER VT-1 receive FDA 510(k) clearance?

ADULT VENTILATOR TESTER VT-1 received FDA 510(k) clearance on 1985-12-03, under 510(k) number K853760.

Who is the listed applicant for ADULT VENTILATOR TESTER VT-1?

The FDA 510(k) record lists Bio-Tek Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADULT VENTILATOR TESTER VT-1?

The FDA product code for ADULT VENTILATOR TESTER VT-1 is CBK.

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 Bio-Tek Instruments, 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 37 devices →

Related Devices (Code: CBK)

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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