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FDA 510(k)

ATRAUCLIP (TANTALUM HEMOSTATIC CLIP)

K-Number: K896998 · 1990-06-01

ApplicantS.P.K. Technology, Inc.
Decision Date1990-06-01
Product CodeMCH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATRAUCLIP (TANTALUM HEMOSTATIC CLIP) is the device name listed in this FDA 510(k) record. The listed applicant is S.P.K. Technology, Inc.. It received FDA 510(k) clearance on 1990-06-01 under 510(k) number K896998. The device is classified under product code MCH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRAUCLIP (TANTALUM HEMOSTATIC CLIP)?

ATRAUCLIP (TANTALUM HEMOSTATIC CLIP) is a medical device that received FDA 510(k) clearance on 1990-06-01. The listed applicant is S.P.K. Technology, Inc.. The 510(k) number is K896998.

When did ATRAUCLIP (TANTALUM HEMOSTATIC CLIP) receive FDA 510(k) clearance?

ATRAUCLIP (TANTALUM HEMOSTATIC CLIP) received FDA 510(k) clearance on 1990-06-01, under 510(k) number K896998.

Who is the listed applicant for ATRAUCLIP (TANTALUM HEMOSTATIC CLIP)?

The FDA 510(k) record lists S.P.K. Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATRAUCLIP (TANTALUM HEMOSTATIC CLIP)?

The FDA product code for ATRAUCLIP (TANTALUM HEMOSTATIC CLIP) is MCH.

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.

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Other records listing S.P.K. Technology, 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.

K896997ATRAUCLIP (TITANIUM HEMOSTATIC CLIP)

Related Devices (Code: MCH)

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.

K040148RESOLUTION HEMOSTASIS CLIPPING DEVICEBoston Scientific CorpK972745TITANIUM HEMOSTATIC CLIPEisner USA, 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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