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FDA 510(k)

REUSABLE HAND-TROL

K-Number: K800597 · 1980-04-02

ApplicantAspen Laboratories, Inc.
Decision Date1980-04-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REUSABLE HAND-TROL is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800597. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE HAND-TROL?

REUSABLE HAND-TROL is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K800597.

When did REUSABLE HAND-TROL receive FDA 510(k) clearance?

REUSABLE HAND-TROL received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800597.

Who is the listed applicant for REUSABLE HAND-TROL?

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

What is the FDA product code for REUSABLE HAND-TROL?

The FDA product code for REUSABLE HAND-TROL is GEI.

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Related Devices (Code: GEI)

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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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