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FDA 510(k)

ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS

K-Number: K880274 · 1988-02-05

ApplicantAdvanced Surgical Products, Inc.
Decision Date1988-02-05
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS 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 1988-02-05 under 510(k) number K880274. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS?

ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K880274.

When did ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS receive FDA 510(k) clearance?

ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS received FDA 510(k) clearance on 1988-02-05, under 510(k) number K880274.

Who is the listed applicant for ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS?

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 SCLERAL PLUG FORCEPS?

The FDA product code for ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS is HNR.

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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 HANDPIECEK884556DREYER CURVED ENDOILLUMINATOR

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Related Devices (Code: HNR)

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.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, 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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