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FDA 510(k)

HAND-TROL CONNECTOR EXTENDER

K-Number: K781429 · 1978-08-31

ApplicantAspen Laboratories, Inc.
Decision Date1978-08-31
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HAND-TROL CONNECTOR EXTENDER 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 1978-08-31 under 510(k) number K781429. 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 HAND-TROL CONNECTOR EXTENDER?

HAND-TROL CONNECTOR EXTENDER is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K781429.

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

HAND-TROL CONNECTOR EXTENDER received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781429.

Who is the listed applicant for HAND-TROL CONNECTOR EXTENDER?

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 HAND-TROL CONNECTOR EXTENDER?

The FDA product code for HAND-TROL CONNECTOR EXTENDER is 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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