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FDA 510(k)

3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET

K-Number: K894986 · 1989-12-01

ApplicantNorth American Sterilization & Packaging Co.
Decision Date1989-12-01
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET is the device name listed in this FDA 510(k) record. The listed applicant is North American Sterilization & Packaging Co.. It received FDA 510(k) clearance on 1989-12-01 under 510(k) number K894986. 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 3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET?

3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET is a medical device that received FDA 510(k) clearance on 1989-12-01. The listed applicant is North American Sterilization & Packaging Co.. The 510(k) number is K894986.

When did 3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET receive FDA 510(k) clearance?

3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET received FDA 510(k) clearance on 1989-12-01, under 510(k) number K894986.

Who is the listed applicant for 3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET?

The FDA 510(k) record lists North American Sterilization & Packaging Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET?

The FDA product code for 3-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKET is OCZ.

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Other records listing North American Sterilization & Packaging Co. as applicant

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K964231NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)K963753NASP TRANSPARENT DRESSINGK962352HYDROGEL SKIN DRESSINGK925588NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRIK925593NORTEC STERILE WATER FOR DEVICE IRRIGATIONK925161NORTEC STERILE WATER FOR CATHETER BALLOON INFLATIO

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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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