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FDA 510(k)

NOVAK CURETTE

K-Number: K854899 · 1985-12-24

ApplicantEuro-Med Intl.
Decision Date1985-12-24
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NOVAK CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Euro-Med Intl.. It received FDA 510(k) clearance on 1985-12-24 under 510(k) number K854899. 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 NOVAK CURETTE?

NOVAK CURETTE is a medical device that received FDA 510(k) clearance on 1985-12-24. The listed applicant is Euro-Med Intl.. The 510(k) number is K854899.

When did NOVAK CURETTE receive FDA 510(k) clearance?

NOVAK CURETTE received FDA 510(k) clearance on 1985-12-24, under 510(k) number K854899.

Who is the listed applicant for NOVAK CURETTE?

The FDA 510(k) record lists Euro-Med Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVAK CURETTE?

The FDA product code for NOVAK CURETTE is FZS.

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Other records listing Euro-Med Intl. 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.

K883884PROSTATIC CORE-CUT NEEDLEK882404KEVOR-CURETTEK854894SPOONK854890HOOK PROBEK854901PACIFIC GRASPERK854891KNIFE

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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.

K932493SURGICAL CURETTEWhitney Products, Inc.K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDKevtek Medical Products, Inc.K892521CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVECymed, Inc.K891888CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPERZinnanti Surgical Instruments, Inc.K891334ACU-CURETTEAcuderm, Inc.K890366ADENOID CURETTEKinetic Medical Products

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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