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FDA 510(k)

PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG

K-Number: K852560 · 1985-06-28

ApplicantThe Huxley Instrument Corp.
Decision Date1985-06-28
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG is the device name listed in this FDA 510(k) record. The listed applicant is The Huxley Instrument Corp.. It received FDA 510(k) clearance on 1985-06-28 under 510(k) number K852560. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG?

PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG is a medical device that received FDA 510(k) clearance on 1985-06-28. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852560.

When did PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG receive FDA 510(k) clearance?

PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG received FDA 510(k) clearance on 1985-06-28, under 510(k) number K852560.

Who is the listed applicant for PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG?

The FDA 510(k) record lists The Huxley Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG?

The FDA product code for PINSET, BONE, RUSH 9-1/2 THRU 20-3/4 INCHES LONG is HTY.

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Other records listing The Huxley Instrument Corp. 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.

K852721BOZEMAN UTERINE FORCEPS, STRAIGHT, 10+410 0R 420K852993BONE RONGEURSK853016STILLE ANGULAR RONGEUR, 8-3/4 SS 410K853015SELF-CENTERING BONE HOLDING FORCEPS, 10-1/4 SS420K852716TAYLOR PERCUSSION HAMMER SS 410 OR 420K852728KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SS

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Related Devices (Code: HTY)

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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