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FDA 510(k)

PRISMA DISPOSABLE J-SHAPED I/A CANNULA

K-Number: K874981 · 1988-04-13

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

Device Summary

PRISMA DISPOSABLE J-SHAPED I/A CANNULA 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 K874981. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRISMA DISPOSABLE J-SHAPED I/A CANNULA?

PRISMA DISPOSABLE J-SHAPED I/A CANNULA 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 K874981.

When did PRISMA DISPOSABLE J-SHAPED I/A CANNULA receive FDA 510(k) clearance?

PRISMA DISPOSABLE J-SHAPED I/A CANNULA received FDA 510(k) clearance on 1988-04-13, under 510(k) number K874981.

Who is the listed applicant for PRISMA DISPOSABLE J-SHAPED I/A CANNULA?

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 J-SHAPED I/A CANNULA?

The FDA product code for PRISMA DISPOSABLE J-SHAPED I/A CANNULA is HMX.

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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: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, 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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