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FDA 510(k)

SOLUTION ADMINISTRATION LINE W/SPIKE

K-Number: K833178 · 1983-11-30

Decision Date1983-11-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLUTION ADMINISTRATION LINE W/SPIKE is the device name listed in this FDA 510(k) record. The listed applicant is Intramed, Inc.. It received FDA 510(k) clearance on 1983-11-30 under 510(k) number K833178. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLUTION ADMINISTRATION LINE W/SPIKE?

SOLUTION ADMINISTRATION LINE W/SPIKE is a medical device that received FDA 510(k) clearance on 1983-11-30. The listed applicant is Intramed, Inc.. The 510(k) number is K833178.

When did SOLUTION ADMINISTRATION LINE W/SPIKE receive FDA 510(k) clearance?

SOLUTION ADMINISTRATION LINE W/SPIKE received FDA 510(k) clearance on 1983-11-30, under 510(k) number K833178.

Who is the listed applicant for SOLUTION ADMINISTRATION LINE W/SPIKE?

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

What is the FDA product code for SOLUTION ADMINISTRATION LINE W/SPIKE?

The FDA product code for SOLUTION ADMINISTRATION LINE W/SPIKE is FPA.

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.

Related Devices (Code: FPA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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