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FDA 510(k)

PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK

K-Number: K875006 · 1988-03-14

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

Device Summary

PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK 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 K875006. 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 DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK?

PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK 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 K875006.

When did PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK receive FDA 510(k) clearance?

PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK received FDA 510(k) clearance on 1988-03-14, under 510(k) number K875006.

Who is the listed applicant for PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK?

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 DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK?

The FDA product code for PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK 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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