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FDA 510(k)

DREYER CURVED ENDOILLUMINATOR

K-Number: K884556 · 1989-02-28

ApplicantAdvanced Surgical Products, Inc.
Decision Date1989-02-28
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DREYER CURVED ENDOILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Products, Inc.. It received FDA 510(k) clearance on 1989-02-28 under 510(k) number K884556. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DREYER CURVED ENDOILLUMINATOR?

DREYER CURVED ENDOILLUMINATOR is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K884556.

When did DREYER CURVED ENDOILLUMINATOR receive FDA 510(k) clearance?

DREYER CURVED ENDOILLUMINATOR received FDA 510(k) clearance on 1989-02-28, under 510(k) number K884556.

Who is the listed applicant for DREYER CURVED ENDOILLUMINATOR?

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

What is the FDA product code for DREYER CURVED ENDOILLUMINATOR?

The FDA product code for DREYER CURVED ENDOILLUMINATOR is HQE.

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Other records listing Advanced Surgical Products, 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.

K030926FAST THROW STAINLESS STEEL SURGICAL SUTUREK895800ADVANCED SURGICAL SOLID STATE BIPOLAR COAGULATORK896754I/A HANDPIECEK896305MULTI-USE I/A HANDPIECEK884557ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECEK890398RYAN-STYLE DIRECTED INFUSION MANIPULATOR

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Related Devices (Code: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, Inc.

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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