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FDA 510(k)

MILL-ROSE ROTATABLE POLYPECTOMY SNARE

K-Number: K951600 · 1995-12-18

ApplicantMill-Rose Laboratory
Decision Date1995-12-18
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MILL-ROSE ROTATABLE POLYPECTOMY SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1995-12-18 under 510(k) number K951600. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILL-ROSE ROTATABLE POLYPECTOMY SNARE?

MILL-ROSE ROTATABLE POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 1995-12-18. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K951600.

When did MILL-ROSE ROTATABLE POLYPECTOMY SNARE receive FDA 510(k) clearance?

MILL-ROSE ROTATABLE POLYPECTOMY SNARE received FDA 510(k) clearance on 1995-12-18, under 510(k) number K951600.

Who is the listed applicant for MILL-ROSE ROTATABLE POLYPECTOMY SNARE?

The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILL-ROSE ROTATABLE POLYPECTOMY SNARE?

The FDA product code for MILL-ROSE ROTATABLE POLYPECTOMY SNARE is FDI.

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Other records listing Mill-Rose Laboratory 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.

K983122MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) COMBINATION CYTOLOGY/HISTOLOGY PROCEDURAL KITK983124MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KITK971275MILL-ROSE DISPOSABLE POLYPECTOMY SNAREK962736MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLEK960880MILL-ROSE BLIND MICROBIOLOGY BRUSHK954519WANG TRANSENDOSCOPIC ASPIRATION NEEDLE

View all 46 devices →

Related Devices (Code: FDI)

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.

K251692Advanced Tissue Resection DeviceMicro-Tech (Nanjing) Co., Ltd.K221713Polypectomy SnareHangzhou AGS MedTech Co., Ltd.K220846CORE-SNAREIncore Co., Ltd.K220089Disposable Polyp SnareJiangsu Vedkang Medical Science and Technology Co., Ltd.K220790Disposable Polypectomy Snare, Disposable Polypectomy Hybrid SnareYangzhou Fartley Medical Instrument Technology Co., Ltd.K213222Disposable Polypectomy SnareBeijing Zksk Technology Co., Ltd.

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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