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FDA 510(k)

POET IQ WITH FIVE AGENT CAPABILITY

K-Number: K942737 · 1995-02-09

Decision Date1995-02-09
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POET IQ WITH FIVE AGENT CAPABILITY is the device name listed in this FDA 510(k) record. The listed applicant is Criticare Systems, Inc.. It received FDA 510(k) clearance on 1995-02-09 under 510(k) number K942737. 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 POET IQ WITH FIVE AGENT CAPABILITY?

POET IQ WITH FIVE AGENT CAPABILITY is a medical device that received FDA 510(k) clearance on 1995-02-09. The listed applicant is Criticare Systems, Inc.. The 510(k) number is K942737.

When did POET IQ WITH FIVE AGENT CAPABILITY receive FDA 510(k) clearance?

POET IQ WITH FIVE AGENT CAPABILITY received FDA 510(k) clearance on 1995-02-09, under 510(k) number K942737.

Who is the listed applicant for POET IQ WITH FIVE AGENT CAPABILITY?

The FDA 510(k) record lists Criticare Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POET IQ WITH FIVE AGENT CAPABILITY?

The FDA product code for POET IQ WITH FIVE AGENT CAPABILITY 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 Criticare Systems, 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 22 devices →

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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