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FDA 510(k)

CRICKET 2000 RECORDING PULSE OXIMETER

K-Number: K972829 · 1997-10-28

Decision Date1997-10-28
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CRICKET 2000 RECORDING PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1997-10-28 under 510(k) number K972829. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRICKET 2000 RECORDING PULSE OXIMETER?

CRICKET 2000 RECORDING PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1997-10-28. The listed applicant is Respironics, Inc.. The 510(k) number is K972829.

When did CRICKET 2000 RECORDING PULSE OXIMETER receive FDA 510(k) clearance?

CRICKET 2000 RECORDING PULSE OXIMETER received FDA 510(k) clearance on 1997-10-28, under 510(k) number K972829.

Who is the listed applicant for CRICKET 2000 RECORDING PULSE OXIMETER?

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

What is the FDA product code for CRICKET 2000 RECORDING PULSE OXIMETER?

The FDA product code for CRICKET 2000 RECORDING PULSE OXIMETER is DQA.

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 Respironics, 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 166 devices →

Related Devices (Code: DQA)

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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