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FDA 510(k)

6203

K-Number: K022865 · 2003-02-13

ApplicantContemporary Products, Inc.
Decision Date2003-02-13
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

6203 is the device name listed in this FDA 510(k) record. The listed applicant is Contemporary Products, Inc.. It received FDA 510(k) clearance on 2003-02-13 under 510(k) number K022865. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 6203?

6203 is a medical device that received FDA 510(k) clearance on 2003-02-13. The listed applicant is Contemporary Products, Inc.. The 510(k) number is K022865.

When did 6203 receive FDA 510(k) clearance?

6203 received FDA 510(k) clearance on 2003-02-13, under 510(k) number K022865.

Who is the listed applicant for 6203?

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

What is the FDA product code for 6203?

The FDA product code for 6203 is NFB.

Other records listing Contemporary Products, 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.

K992935OCD2001K000543CONTEMPRO-MISTK964994CPI MODEL 6240 50 PSI NEBULIZER COMPRESSORK963558CPI MODEL 6260, 6260A OR 6261 OIL-LESS ASPIRATOR

Related Devices (Code: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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