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FDA 510(k)

SUNDT AVM MICRO CLIP

K-Number: K902544 · 1990-09-20

ApplicantCodman & Shurtleff, Inc.
Decision Date1990-09-20
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SUNDT AVM MICRO CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K902544. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNDT AVM MICRO CLIP?

SUNDT AVM MICRO CLIP is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K902544.

When did SUNDT AVM MICRO CLIP receive FDA 510(k) clearance?

SUNDT AVM MICRO CLIP received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902544.

Who is the listed applicant for SUNDT AVM MICRO CLIP?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNDT AVM MICRO CLIP?

The FDA product code for SUNDT AVM MICRO CLIP is HCI.

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Related Devices (Code: HCI)

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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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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