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FDA 510(k)

SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE

K-Number: K850267 · 1985-02-27

ApplicantSparco, Inc.
Decision Date1985-02-27
Product Code
DecisionSubstantially Equivalent

Device Summary

SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE is the device name listed in this FDA 510(k) record. The listed applicant is Sparco, Inc.. It received FDA 510(k) clearance on 1985-02-27 under 510(k) number K850267. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE?

SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Sparco, Inc.. The 510(k) number is K850267.

When did SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE receive FDA 510(k) clearance?

SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850267.

Who is the listed applicant for SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE?

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

Related Clinical Trials

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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Other records listing Sparco, 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.

K884041MASTER-GUARDK863964LIMB-GUARDK850268SPARCO SCOPE GUARDK844286FLASH GUARD PLASTIC VERSIONK841669FLASH GUARD

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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