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FDA 510(k)

DISP. GROUND PAD PREGELLED

K-Number: K771329 · 1977-09-06

ApplicantEdward Weck, Inc.
Decision Date1977-09-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. GROUND PAD PREGELLED 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 1977-09-06 under 510(k) number K771329. 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 DISP. GROUND PAD PREGELLED?

DISP. GROUND PAD PREGELLED is a medical device that received FDA 510(k) clearance on 1977-09-06. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771329.

When did DISP. GROUND PAD PREGELLED receive FDA 510(k) clearance?

DISP. GROUND PAD PREGELLED received FDA 510(k) clearance on 1977-09-06, under 510(k) number K771329.

Who is the listed applicant for DISP. GROUND PAD PREGELLED?

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 DISP. GROUND PAD PREGELLED?

The FDA product code for DISP. GROUND PAD PREGELLED 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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