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FDA 510(k)

ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE

K-Number: K884557 · 1989-05-12

ApplicantAdvanced Surgical Products, Inc.
Decision Date1989-05-12
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE 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 1989-05-12 under 510(k) number K884557. 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 ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE?

ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE is a medical device that received FDA 510(k) clearance on 1989-05-12. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K884557.

When did ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE receive FDA 510(k) clearance?

ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE received FDA 510(k) clearance on 1989-05-12, under 510(k) number K884557.

Who is the listed applicant for ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE?

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 ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE?

The FDA product code for ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE 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 HANDPIECEK884556DREYER CURVED ENDOILLUMINATORK890398RYAN-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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