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FDA 510(k)

I.V. START KIT

K-Number: K932071 · 1994-02-17

ApplicantClinipad Corp.
Decision Date1994-02-17
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clinipad Corp.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K932071. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. START KIT?

I.V. START KIT is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Clinipad Corp.. The 510(k) number is K932071.

When did I.V. START KIT receive FDA 510(k) clearance?

I.V. START KIT received FDA 510(k) clearance on 1994-02-17, under 510(k) number K932071.

Who is the listed applicant for I.V. START KIT?

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

What is the FDA product code for I.V. START KIT?

The FDA product code for I.V. START KIT is FOZ.

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Other records listing Clinipad 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.

K931560CARDIAC CATHETERIZATION TRAYK931668PICC INSERTION TRAYK932010V.A.D. ACCESS KITK932036LACERATION TRAYK932016TRACHEOSTOMY CARE TRAYK862562PUNCH BIOPSY KIT

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Related Devices (Code: FOZ)

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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