FDA 510(k)

SOLUTION TRANSFER CONTAINER

K-Number: K830299 · 1983-02-19

ApplicantThe Healthcare Group Laboratories, Inc.

Decision Date1983-02-19

Product CodeKPE

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

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 1983-02-19 under 510(k) number K830299. 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 SOLUTION TRANSFER CONTAINER?

SOLUTION TRANSFER CONTAINER is a medical device that received FDA 510(k) clearance on 1983-02-19. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K830299.

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

SOLUTION TRANSFER CONTAINER received FDA 510(k) clearance on 1983-02-19, under 510(k) number K830299.

Who is the listed applicant for 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 SOLUTION TRANSFER CONTAINER?

The FDA product code for SOLUTION TRANSFER CONTAINER is KPE.

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Other records listing The Healthcare Group Laboratories, Inc. as applicant

K850035EMPTY SOLUTION TRANSFER CONTAINER K842170EMPTY SOLUTION TRANSFER CONTAINER K842091DISPOS. ACU-CUT SOFT TISSUE BIOPSY K840742RIGHT ATRIAL CATHETER K822307ADHESIVE SPRAY #4050-4060 K822059SHOW'RBAG

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Related Devices (Code: KPE)

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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.