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FDA 510(k)

WECK TROCAR

K-Number: K915378 · 1992-06-29

ApplicantEdward Weck, Inc.
Decision Date1992-06-29
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WECK TROCAR 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 1992-06-29 under 510(k) number K915378. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WECK TROCAR?

WECK TROCAR is a medical device that received FDA 510(k) clearance on 1992-06-29. The listed applicant is Edward Weck, Inc.. The 510(k) number is K915378.

When did WECK TROCAR receive FDA 510(k) clearance?

WECK TROCAR received FDA 510(k) clearance on 1992-06-29, under 510(k) number K915378.

Who is the listed applicant for WECK TROCAR?

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 WECK TROCAR?

The FDA product code for WECK TROCAR is HET.

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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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