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FDA 510(k)

SCALPEL HANDLE #7 SS 410 OR 420

K-Number: K852735 · 1985-07-15

Decision Date1985-07-15
Product CodeGDZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SCALPEL HANDLE #7 SS 410 OR 420 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 1985-07-15 under 510(k) number K852735. The device is classified under product code GDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCALPEL HANDLE #7 SS 410 OR 420?

SCALPEL HANDLE #7 SS 410 OR 420 is a medical device that received FDA 510(k) clearance on 1985-07-15. The listed applicant is The Huxley Instrument Corp.. The 510(k) number is K852735.

When did SCALPEL HANDLE #7 SS 410 OR 420 receive FDA 510(k) clearance?

SCALPEL HANDLE #7 SS 410 OR 420 received FDA 510(k) clearance on 1985-07-15, under 510(k) number K852735.

Who is the listed applicant for SCALPEL HANDLE #7 SS 410 OR 420?

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 SCALPEL HANDLE #7 SS 410 OR 420?

The FDA product code for SCALPEL HANDLE #7 SS 410 OR 420 is GDZ.

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.

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.

View all 53 devices →

Related Devices (Code: GDZ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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