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FDA 510(k)

HEMOSPENSER CARTRIDGE CAT. NO. 523500-

K-Number: K792378 · 1979-12-06

ApplicantEdward Weck, Inc.
Decision Date1979-12-06
Product CodeGDO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEMOSPENSER CARTRIDGE CAT. NO. 523500- 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 1979-12-06 under 510(k) number K792378. The device is classified under product code GDO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOSPENSER CARTRIDGE CAT. NO. 523500-?

HEMOSPENSER CARTRIDGE CAT. NO. 523500- is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Edward Weck, Inc.. The 510(k) number is K792378.

When did HEMOSPENSER CARTRIDGE CAT. NO. 523500- receive FDA 510(k) clearance?

HEMOSPENSER CARTRIDGE CAT. NO. 523500- received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792378.

Who is the listed applicant for HEMOSPENSER CARTRIDGE CAT. NO. 523500-?

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 HEMOSPENSER CARTRIDGE CAT. NO. 523500-?

The FDA product code for HEMOSPENSER CARTRIDGE CAT. NO. 523500- is GDO.

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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: GDO)

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.

K926199UNICLIP SURGICAL CLIP APPLIERUnisurge, Inc.K890941MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APPUnited States Surgical, A Division of Tyco HealthcK890159TOWEL CLIPSDhason Brothers, Inc.K890233SUTURE CLIP APPLIER/REMOVERKinetic Medical ProductsK820837DISPOSABLE MULTIPLE LIGATING CLIPETHICON, Inc.K812291ETHICON MULTIPLE LIGATING CLIP APPLIERETHICON, Inc.

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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