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FDA 510(k)

DERMAHOOK #382-805

K-Number: K771187 · 1977-07-11

ApplicantEdward Weck, Inc.
Decision Date1977-07-11
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMAHOOK #382-805 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 1977-07-11 under 510(k) number K771187. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAHOOK #382-805?

DERMAHOOK #382-805 is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771187.

When did DERMAHOOK #382-805 receive FDA 510(k) clearance?

DERMAHOOK #382-805 received FDA 510(k) clearance on 1977-07-11, under 510(k) number K771187.

Who is the listed applicant for DERMAHOOK #382-805?

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 DERMAHOOK #382-805?

The FDA product code for DERMAHOOK #382-805 is GDG.

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Other records listing Edward Weck, Inc. as applicant

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

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Related Devices (Code: GDG)

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.

K900069MODIFIED PGL ABSORBABLE STAPLE*United States Surgical, A Division of Tyco HealthcK891898SKIN HOOKS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K864425RAYLOR(TM) DISSECTING HOOKCedar Surgical, Inc.K843136BRIMFIELD CANNULATED GRASPING HOOKSBrimfield Scientific InstrumentsK841010SURGICAL HOOKS, VARIOUSPremier Dental Products Co.K812562SURGICAL RETRACTOR & ELASTIC STAYS, DISPHumboldt Products

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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