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FDA 510(k)

HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM

K-Number: K051276 · 2005-10-28

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date2005-10-28
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2005-10-28 under 510(k) number K051276. 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 HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM?

HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM is a medical device that received FDA 510(k) clearance on 2005-10-28. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K051276.

When did HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM receive FDA 510(k) clearance?

HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM received FDA 510(k) clearance on 2005-10-28, under 510(k) number K051276.

Who is the listed applicant for HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM?

The FDA product code for HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM is OCZ.

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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.

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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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