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FDA 510(k)

PRISMA DISPOSABLE ENDO-OCULAR PROBE

K-Number: K875000 · 1988-04-13

ApplicantAdvanced Surgical Products, Inc.
Decision Date1988-04-13
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PRISMA DISPOSABLE ENDO-OCULAR PROBE 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 1988-04-13 under 510(k) number K875000. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRISMA DISPOSABLE ENDO-OCULAR PROBE?

PRISMA DISPOSABLE ENDO-OCULAR PROBE is a medical device that received FDA 510(k) clearance on 1988-04-13. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K875000.

When did PRISMA DISPOSABLE ENDO-OCULAR PROBE receive FDA 510(k) clearance?

PRISMA DISPOSABLE ENDO-OCULAR PROBE received FDA 510(k) clearance on 1988-04-13, under 510(k) number K875000.

Who is the listed applicant for PRISMA DISPOSABLE ENDO-OCULAR PROBE?

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 DISPOSABLE ENDO-OCULAR PROBE?

The FDA product code for PRISMA DISPOSABLE ENDO-OCULAR PROBE is HQF.

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Other records listing Advanced Surgical Products, Inc. as applicant

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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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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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