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FDA 510(k)

TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR

K-Number: K863801 · 1987-01-12

Decision Date1987-01-12
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Traverse Medical Monitors. It received FDA 510(k) clearance on 1987-01-12 under 510(k) number K863801. The device is classified under product code CBS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR?

TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR is a medical device that received FDA 510(k) clearance on 1987-01-12. The listed applicant is Traverse Medical Monitors. The 510(k) number is K863801.

When did TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR receive FDA 510(k) clearance?

TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR received FDA 510(k) clearance on 1987-01-12, under 510(k) number K863801.

Who is the listed applicant for TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR?

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

What is the FDA product code for TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR?

The FDA product code for TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR is CBS.

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 Traverse Medical Monitors 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.

Related Devices (Code: CBS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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