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FDA 510(k)

SKIN STAPLE REMOVER KIT

K-Number: K915430 · 1992-02-28

ApplicantCypress Medical Products, Ltd.
Decision Date1992-02-28
Product CodeGDT
Advisory CommitteeSU
DecisionUnknown

Device Summary

SKIN STAPLE REMOVER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cypress Medical Products, Ltd.. It received FDA 510(k) clearance on 1992-02-28 under 510(k) number K915430. The device is classified under product code GDT. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SKIN STAPLE REMOVER KIT?

SKIN STAPLE REMOVER KIT is a medical device that received FDA 510(k) clearance on 1992-02-28. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K915430.

When did SKIN STAPLE REMOVER KIT receive FDA 510(k) clearance?

SKIN STAPLE REMOVER KIT received FDA 510(k) clearance on 1992-02-28, under 510(k) number K915430.

Who is the listed applicant for SKIN STAPLE REMOVER KIT?

The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIN STAPLE REMOVER KIT?

The FDA product code for SKIN STAPLE REMOVER KIT is GDT.

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Other records listing Cypress Medical Products, Ltd. 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.

K021676CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METALK012282STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVEK972899CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETERK972849ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)K972883ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)K952367CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE

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Related Devices (Code: GDT)

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.

K963234STAPLE REMOVAL KITContinental Medical Laboratories, Inc.K943719VISISTAT STAPLERPilling Weck, Inc.K925526MANIPLER DISPOSABLE SKIN STAPLERMatsutani Seisakusho Co. , Ltd.K911204QUALTEX SKIN STAPLE EXTRACTORDeroyal Industries, Inc.K910586AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER*United States Surgical, A Division of Tyco HealthcK900486APPOSE UNITY STERILE DISPOSABLE SKIN STAPLERDavis & Geck, 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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