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FDA 510(k)

LUNE AU CURETTES

K-Number: K850068 · 1985-04-08

ApplicantLuneau Laboratories
Decision Date1985-04-08
Product CodeHCY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LUNE AU CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is Luneau Laboratories. It received FDA 510(k) clearance on 1985-04-08 under 510(k) number K850068. The device is classified under product code HCY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNE AU CURETTES?

LUNE AU CURETTES is a medical device that received FDA 510(k) clearance on 1985-04-08. The listed applicant is Luneau Laboratories. The 510(k) number is K850068.

When did LUNE AU CURETTES receive FDA 510(k) clearance?

LUNE AU CURETTES received FDA 510(k) clearance on 1985-04-08, under 510(k) number K850068.

Who is the listed applicant for LUNE AU CURETTES?

The FDA 510(k) record lists Luneau Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUNE AU CURETTES?

The FDA product code for LUNE AU CURETTES is HCY.

Related Clinical Trials

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Other records listing Luneau Laboratories 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.

K844365COLOR VISION TESTERSK844364SKIASCOPIC RACKSK844362OPHTHALMIC CHAIRK844363OPHTHALMIC STAND

Related Devices (Code: HCY)

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.

K980096OAC (OPTICAL ASPIRATING CURETTE)Imagyn Medical Technologies, Inc.K944238ENDOCYTE TMD.L. Nelson and Assoc., Inc.K935822PHASE I CURETTEPhase I Corp.K901442BAXTER D & C TRAYBaxter Healthcare CorpK890384UTERINE CURETTEKinetic Medical ProductsK881794IVORY FINDER SETIvory Instruments Co.

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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