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FDA 510(k)

NEW SIZES SUGITA CLIPS

K-Number: K881911 · 1988-06-06

ApplicantDowns Surgical , Ltd.
Decision Date1988-06-06
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEW SIZES SUGITA CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1988-06-06 under 510(k) number K881911. 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 NEW SIZES SUGITA CLIPS?

NEW SIZES SUGITA CLIPS is a medical device that received FDA 510(k) clearance on 1988-06-06. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K881911.

When did NEW SIZES SUGITA CLIPS receive FDA 510(k) clearance?

NEW SIZES SUGITA CLIPS received FDA 510(k) clearance on 1988-06-06, under 510(k) number K881911.

Who is the listed applicant for NEW SIZES SUGITA CLIPS?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW SIZES SUGITA CLIPS?

The FDA product code for NEW SIZES SUGITA CLIPS is HCI.

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Other records listing Downs Surgical , Ltd. as applicant

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Related Devices (Code: HCI)

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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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