FDA 510(k)

HEPARIN LOCK FLUSH SOLUTION USP KIT,100

K-Number: K841306 · 1984-06-04

Decision Date1984-06-04

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HEPARIN LOCK FLUSH SOLUTION USP KIT,100 is the device name listed in this FDA 510(k) record. The listed applicant is Solo Pak Laboratories. It received FDA 510(k) clearance on 1984-06-04 under 510(k) number K841306. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEPARIN LOCK FLUSH SOLUTION USP KIT,100?

HEPARIN LOCK FLUSH SOLUTION USP KIT,100 is a medical device that received FDA 510(k) clearance on 1984-06-04. The listed applicant is Solo Pak Laboratories. The 510(k) number is K841306.

When did HEPARIN LOCK FLUSH SOLUTION USP KIT,100 receive FDA 510(k) clearance?

HEPARIN LOCK FLUSH SOLUTION USP KIT,100 received FDA 510(k) clearance on 1984-06-04, under 510(k) number K841306.

Who is the listed applicant for HEPARIN LOCK FLUSH SOLUTION USP KIT,100?

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

What is the FDA product code for HEPARIN LOCK FLUSH SOLUTION USP KIT,100?

The FDA product code for HEPARIN LOCK FLUSH SOLUTION USP KIT,100 is FMI.

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 Solo Pak Laboratories as applicant

K851944MAX-I-PROBE HANDPIECE K841166HEPARIN LOCK FLUSH PROCEDURE PACK K841305HEPARIN LOCK FLUSH SOLUTION USP KIT

Related Devices (Code: FMI)

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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.