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FDA 510(k)

PRECISION - COSMET CAPSULE COUPEUR

K-Number: K852934 · 1985-08-08

ApplicantPrecision-Cosmet Co., Inc.
Decision Date1985-08-08
Product CodeHNY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PRECISION - COSMET CAPSULE COUPEUR is the device name listed in this FDA 510(k) record. The listed applicant is Precision-Cosmet Co., Inc.. It received FDA 510(k) clearance on 1985-08-08 under 510(k) number K852934. The device is classified under product code HNY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION - COSMET CAPSULE COUPEUR?

PRECISION - COSMET CAPSULE COUPEUR is a medical device that received FDA 510(k) clearance on 1985-08-08. The listed applicant is Precision-Cosmet Co., Inc.. The 510(k) number is K852934.

When did PRECISION - COSMET CAPSULE COUPEUR receive FDA 510(k) clearance?

PRECISION - COSMET CAPSULE COUPEUR received FDA 510(k) clearance on 1985-08-08, under 510(k) number K852934.

Who is the listed applicant for PRECISION - COSMET CAPSULE COUPEUR?

The FDA 510(k) record lists Precision-Cosmet Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION - COSMET CAPSULE COUPEUR?

The FDA product code for PRECISION - COSMET CAPSULE COUPEUR is HNY.

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.

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Other records listing Precision-Cosmet Co., 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.

K861057MANUAL OPHTHALMIC SURGICAL INSTRUMENTSK840204WHITE OCULAR PRESSURE RELIEF DEVICEK840104PETRUS IOL GUIDE

Related Devices (Code: HNY)

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.

K961524STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORSSterilab, Inc.K880345CYSTOTOMES/KNIFESMyocure, Inc.K874993PRISMA DISPOSABLE SHARP IRRIGATING CYSTOTOMEAdvanced Surgical Products, Inc.K874997PRISMA DISPOSABLE STRAIGHT IRRIGATING CYSTOTOMEAdvanced Surgical Products, Inc.K874983PRISMA DISPOSABLE ANGLED IRRIGATING CYSTOTOMEAdvanced Surgical Products, Inc.K874975PRISMA DISPOSABLE SHARP ANGLED IRRIGAT. CYSTOTOMEAdvanced Surgical Products, Inc.

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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