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FDA 510(k)

THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K

K-Number: K852937 · 1985-07-26

ApplicantNorthern Customfab, Inc.
Decision Date1985-07-26
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K is the device name listed in this FDA 510(k) record. The listed applicant is Northern Customfab, Inc.. It received FDA 510(k) clearance on 1985-07-26 under 510(k) number K852937. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K?

THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K is a medical device that received FDA 510(k) clearance on 1985-07-26. The listed applicant is Northern Customfab, Inc.. The 510(k) number is K852937.

When did THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K receive FDA 510(k) clearance?

THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K received FDA 510(k) clearance on 1985-07-26, under 510(k) number K852937.

Who is the listed applicant for THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K?

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

What is the FDA product code for THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K?

The FDA product code for THE IVY POLE-INTRAVENOUS BOT TREES #1121K & 1221K is FOX.

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Other records listing Northern Customfab, 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.

K852938TUF TRACK MODEL TT83 CUBICLE TRACK & IV83 INTR TRK

Related Devices (Code: FOX)

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.

K980336IV STANDSClinton Industries, Inc.K964782MEDRAD CONTRAST HOLDERMedrad, Inc.K961470PORT-A-POLEPrins Medical Ind., Inc.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.K950367IV SHUTTLEEquipment Concepts, Inc.

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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