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FDA 510(k)

DANDY HEMOSTATIC FORCEPS

K-Number: K772389 · 1978-01-06

ApplicantEdward Weck, Inc.
Decision Date1978-01-06
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DANDY HEMOSTATIC FORCEPS 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 1978-01-06 under 510(k) number K772389. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANDY HEMOSTATIC FORCEPS?

DANDY HEMOSTATIC FORCEPS is a medical device that received FDA 510(k) clearance on 1978-01-06. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772389.

When did DANDY HEMOSTATIC FORCEPS receive FDA 510(k) clearance?

DANDY HEMOSTATIC FORCEPS received FDA 510(k) clearance on 1978-01-06, under 510(k) number K772389.

Who is the listed applicant for DANDY HEMOSTATIC FORCEPS?

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 DANDY HEMOSTATIC FORCEPS?

The FDA product code for DANDY HEMOSTATIC FORCEPS is HAO.

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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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