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FDA 510(k)

LOOP RETRIEVER

K-Number: K830802 · 1983-04-28

ApplicantVan-Tec, Inc.
Decision Date1983-04-28
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LOOP RETRIEVER is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830802. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOOP RETRIEVER?

LOOP RETRIEVER is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Van-Tec, Inc.. The 510(k) number is K830802.

When did LOOP RETRIEVER receive FDA 510(k) clearance?

LOOP RETRIEVER received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830802.

Who is the listed applicant for LOOP RETRIEVER?

The FDA 510(k) record lists Van-Tec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOOP RETRIEVER?

The FDA product code for LOOP RETRIEVER is OCZ.

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Other records listing Van-Tec, Inc. as applicant

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Related Devices (Code: OCZ)

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.

K252800KARL STORZ Endoscopic Accessories for UrologyKarl Storz SE & CO. KGK242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter (SC500230)Envision EndoscopyK191900Single Use Grasping ForcepsZhejiang Chuangxiang Medical Technology Co., Ltd.K152802Grasping ForcepsMicro-Tech (Nanjing) Co., Ltd.K120084ENDOSCOPIC RETRIEVAL DEVICEUnited States Endoscopy Group, Inc.K103688G-PROX EZ ENDOSCOPIC GRASPERUsgi Medical

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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