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FDA 510(k)

SIMPLICITY SERIES 5

K-Number: K881634 · 1988-05-17

ApplicantQuartet Technology, Inc.
Decision Date1988-05-17
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SIMPLICITY SERIES 5 is the device name listed in this FDA 510(k) record. The listed applicant is Quartet Technology, Inc.. It received FDA 510(k) clearance on 1988-05-17 under 510(k) number K881634. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLICITY SERIES 5?

SIMPLICITY SERIES 5 is a medical device that received FDA 510(k) clearance on 1988-05-17. The listed applicant is Quartet Technology, Inc.. The 510(k) number is K881634.

When did SIMPLICITY SERIES 5 receive FDA 510(k) clearance?

SIMPLICITY SERIES 5 received FDA 510(k) clearance on 1988-05-17, under 510(k) number K881634.

Who is the listed applicant for SIMPLICITY SERIES 5?

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

What is the FDA product code for SIMPLICITY SERIES 5?

The FDA product code for SIMPLICITY SERIES 5 is IQA.

Related Clinical Trials

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Related Devices (Code: IQA)

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.

K961306DELTATALKER WITH INFRAREDPrentke Romich Co.K953905IMPERIUMTeledyne Brown EngineeringK953937LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEMApt Technology, Inc.K943244DEUCEApt Technology, Inc.K944585SCANNING DIRECTORPrentke Romich Co.K944345BEDSIDE BUTLERTrac Medical, Inc.

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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