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FDA 510(k)

LEAD HAND

K-Number: K772387 · 1978-04-05

ApplicantEdward Weck, Inc.
Decision Date1978-04-05
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEAD HAND is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1978-04-05 under 510(k) number K772387. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEAD HAND?

LEAD HAND is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772387.

When did LEAD HAND receive FDA 510(k) clearance?

LEAD HAND received FDA 510(k) clearance on 1978-04-05, under 510(k) number K772387.

Who is the listed applicant for LEAD HAND?

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

What is the FDA product code for LEAD HAND?

The FDA product code for LEAD HAND is KKX.

Other records listing Edward Weck, Inc. as applicant

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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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