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FDA 510(k)

SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK

K-Number: K041017 · 2004-06-25

ApplicantSpsmedical Supply Corp.
Decision Date2004-06-25
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK is the device name listed in this FDA 510(k) record. The listed applicant is Spsmedical Supply Corp.. It received FDA 510(k) clearance on 2004-06-25 under 510(k) number K041017. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK?

SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK is a medical device that received FDA 510(k) clearance on 2004-06-25. The listed applicant is Spsmedical Supply Corp.. The 510(k) number is K041017.

When did SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK receive FDA 510(k) clearance?

SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK received FDA 510(k) clearance on 2004-06-25, under 510(k) number K041017.

Who is the listed applicant for SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK?

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

What is the FDA product code for SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK?

The FDA product code for SPSMEDICAL AIRVIEW BOWIE DICK TEST PACK is JOJ.

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Other records listing Spsmedical Supply 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.

K122024SPSMEDICAL SPORVIEW 10 STEAM SELF CONTAINED BIOLOGICAL INDICATORK130211AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETSK111515SPSMEDICAL SPORVIEW STEAM BIK110152SPSMEDICAL VAPORIZED HYDROGEN PEROXIDE CHEMICAL INDICATORSK102363SPSMEDICAL EMPLUS 270 F STEAM EMULATOR MODEL EMP-104, EMP-1004K090650SPSMEDICAL VAPORIZED HYDROGEN PEROXIDE CHEMICAL INDICATORS

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Related Devices (Code: JOJ)

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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