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FDA 510(k)

EMPTY SOLUTION TRANSFER CONTAINER

K-Number: K842170 · 1984-10-19

Decision Date1984-10-19
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMPTY SOLUTION TRANSFER CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K842170. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMPTY SOLUTION TRANSFER CONTAINER?

EMPTY SOLUTION TRANSFER CONTAINER is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K842170.

When did EMPTY SOLUTION TRANSFER CONTAINER receive FDA 510(k) clearance?

EMPTY SOLUTION TRANSFER CONTAINER received FDA 510(k) clearance on 1984-10-19, under 510(k) number K842170.

Who is the listed applicant for EMPTY SOLUTION TRANSFER CONTAINER?

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

What is the FDA product code for EMPTY SOLUTION TRANSFER CONTAINER?

The FDA product code for EMPTY SOLUTION TRANSFER CONTAINER is KPE.

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.

Other records listing The Healthcare Group Laboratories, 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.

View all 29 devices →

Related Devices (Code: KPE)

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

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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