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FDA 510(k)

NICOLET PORATBLE SPIRIT SYSTEM

K-Number: K915652 · 1992-02-07

ApplicantNicolet Instrument Corp.
Decision Date1992-02-07
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NICOLET PORATBLE SPIRIT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Instrument Corp.. It received FDA 510(k) clearance on 1992-02-07 under 510(k) number K915652. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICOLET PORATBLE SPIRIT SYSTEM?

NICOLET PORATBLE SPIRIT SYSTEM is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Nicolet Instrument Corp.. The 510(k) number is K915652.

When did NICOLET PORATBLE SPIRIT SYSTEM receive FDA 510(k) clearance?

NICOLET PORATBLE SPIRIT SYSTEM received FDA 510(k) clearance on 1992-02-07, under 510(k) number K915652.

Who is the listed applicant for NICOLET PORATBLE SPIRIT SYSTEM?

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

What is the FDA product code for NICOLET PORATBLE SPIRIT SYSTEM?

The FDA product code for NICOLET PORATBLE SPIRIT SYSTEM is GWF.

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Other records listing Nicolet Instrument 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.

K921138NICOLET ULTRASOM ACQUISITION STATIONK923315NICOLET ARK SYSTEMK921927NICOLET VOYAGEURK905632NICOLET MAPLELEAF SYSTEMK897154NICOLET DBTE HEARING AID: DIGITAL & PROGRAMMABLEK894629NICOLET BEAM II SYSTEM

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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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