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FDA 510(k)

GENERAL UTILITY SURG. SCISSORS #460180-

K-Number: K800721 · 1980-05-08

ApplicantEdward Weck, Inc.
Decision Date1980-05-08
Product CodeHRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GENERAL UTILITY SURG. SCISSORS #460180- 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 1980-05-08 under 510(k) number K800721. The device is classified under product code HRR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL UTILITY SURG. SCISSORS #460180-?

GENERAL UTILITY SURG. SCISSORS #460180- is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Edward Weck, Inc.. The 510(k) number is K800721.

When did GENERAL UTILITY SURG. SCISSORS #460180- receive FDA 510(k) clearance?

GENERAL UTILITY SURG. SCISSORS #460180- received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800721.

Who is the listed applicant for GENERAL UTILITY SURG. SCISSORS #460180-?

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 GENERAL UTILITY SURG. SCISSORS #460180-?

The FDA product code for GENERAL UTILITY SURG. SCISSORS #460180- is HRR.

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Other records listing Edward Weck, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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Related Devices (Code: HRR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890212MICROSURGICAL SCISSORSKinetic Medical ProductsK890261TRIGEMINAL SCISSORSKinetic Medical ProductsK890225SURGICAL SCISSORSKinetic Medical ProductsK873502SCISSOR, RIGHTArthropedics, Inc.K873501SCISSOR, LEFTArthropedics, Inc.K85180069-100 TO 69-114 VARIOUS CUTICLE SCISSORSArtiberia

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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