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FDA 510(k)

PRISMA DISPOSABLE KRATZ CAPSULE POLISHER

K-Number: K874969 · 1988-04-13

Decision Date1988-04-13
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PRISMA DISPOSABLE KRATZ CAPSULE POLISHER 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 K874969. 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 KRATZ CAPSULE POLISHER?

PRISMA DISPOSABLE KRATZ CAPSULE POLISHER 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 K874969.

When did PRISMA DISPOSABLE KRATZ CAPSULE POLISHER receive FDA 510(k) clearance?

PRISMA DISPOSABLE KRATZ CAPSULE POLISHER received FDA 510(k) clearance on 1988-04-13, under 510(k) number K874969.

Who is the listed applicant for PRISMA DISPOSABLE KRATZ CAPSULE POLISHER?

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 KRATZ CAPSULE POLISHER?

The FDA product code for PRISMA DISPOSABLE KRATZ CAPSULE POLISHER is HMX.

Related Clinical Trials

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.

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.

View all 64 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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