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FDA 510(k)

ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100

K-Number: K001842 · 2000-09-15

ApplicantSomanetics Corp.
Decision Date2000-09-15
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100 is the device name listed in this FDA 510(k) record. The listed applicant is Somanetics Corp.. It received FDA 510(k) clearance on 2000-09-15 under 510(k) number K001842. 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 ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100?

ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100 is a medical device that received FDA 510(k) clearance on 2000-09-15. The listed applicant is Somanetics Corp.. The 510(k) number is K001842.

When did ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100 receive FDA 510(k) clearance?

ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100 received FDA 510(k) clearance on 2000-09-15, under 510(k) number K001842.

Who is the listed applicant for ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100?

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

What is the FDA product code for ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100?

The FDA product code for ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100 is DQA.

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Other records listing Somanetics Corp. 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.

K093422VITAL SYNC MODEL 5000 SERIESK091224OXYALERT NIRSENSORS, ACCESSORIES FOR INVOS 5100C SYSTEM, MODELS: IS-C AND IS-SK082327INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL: 5100CK080769INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL 5100CK051274INVOS SYSTEMK040162CORRESTORE PATCH SYSTEM

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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.

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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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