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FDA 510(k)

CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER

K-Number: K891888 · 1989-04-12

Decision Date1989-04-12
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-04-12 under 510(k) number K891888. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER?

CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891888.

When did CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER receive FDA 510(k) clearance?

CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER received FDA 510(k) clearance on 1989-04-12, under 510(k) number K891888.

Who is the listed applicant for CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER?

The FDA product code for CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER is FZS.

Related Clinical Trials

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.

Other records listing Zinnanti Surgical Instruments, Inc. 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.

View all 76 devices →

Related Devices (Code: FZS)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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