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FDA 510(k)

PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.

K-Number: K875005 · 1988-03-14

ApplicantAdvanced Surgical Products, Inc.
Decision Date1988-03-14
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA. 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 1988-03-14 under 510(k) number K875005. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.?

PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA. is a medical device that received FDA 510(k) clearance on 1988-03-14. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K875005.

When did PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA. receive FDA 510(k) clearance?

PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA. received FDA 510(k) clearance on 1988-03-14, under 510(k) number K875005.

Who is the listed applicant for PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.?

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 PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.?

The FDA product code for PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA. is FST.

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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: FST)

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.

K200874TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal EndInnovasis, Inc.K122637LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999Stryker SpineK113697EIGR SURGICAL ILLUMINATION SYSTEMInvuity, Inc.K113330CABLECAPSensormedK102266ISOLED AC-POWERED LED HEADLIGHT SYSTEMIsolux, LLCK101496CABLECAP MODEL: WLF, STZ, ACMSensormed

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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