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FDA 510(k)

SHEPPERD STRAIGHT AND CURVED NEEDLES

K-Number: K900609 · 1990-10-22

ApplicantDowns Surgical , Ltd.
Decision Date1990-10-22
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SHEPPERD STRAIGHT AND CURVED NEEDLES 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 1990-10-22 under 510(k) number K900609. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEPPERD STRAIGHT AND CURVED NEEDLES?

SHEPPERD STRAIGHT AND CURVED NEEDLES is a medical device that received FDA 510(k) clearance on 1990-10-22. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K900609.

When did SHEPPERD STRAIGHT AND CURVED NEEDLES receive FDA 510(k) clearance?

SHEPPERD STRAIGHT AND CURVED NEEDLES received FDA 510(k) clearance on 1990-10-22, under 510(k) number K900609.

Who is the listed applicant for SHEPPERD STRAIGHT AND CURVED NEEDLES?

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 SHEPPERD STRAIGHT AND CURVED NEEDLES?

The FDA product code for SHEPPERD STRAIGHT AND CURVED NEEDLES is HRX.

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Other records listing Downs Surgical , Ltd. as applicant

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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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