Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HHI PNEUMATIC ROTARY DRILL

K-Number: K922661 · 1992-09-18

ApplicantH&H Instruments
Decision Date1992-09-18
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HHI PNEUMATIC ROTARY DRILL is the device name listed in this FDA 510(k) record. The listed applicant is H&H Instruments. It received FDA 510(k) clearance on 1992-09-18 under 510(k) number K922661. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HHI PNEUMATIC ROTARY DRILL?

HHI PNEUMATIC ROTARY DRILL is a medical device that received FDA 510(k) clearance on 1992-09-18. The listed applicant is H&H Instruments. The 510(k) number is K922661.

When did HHI PNEUMATIC ROTARY DRILL receive FDA 510(k) clearance?

HHI PNEUMATIC ROTARY DRILL received FDA 510(k) clearance on 1992-09-18, under 510(k) number K922661.

Who is the listed applicant for HHI PNEUMATIC ROTARY DRILL?

The FDA 510(k) record lists H&H Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HHI PNEUMATIC ROTARY DRILL?

The FDA product code for HHI PNEUMATIC ROTARY DRILL is HSZ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing H&H Instruments 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.

K922056HHI ELECTRIC CONSOLE #875-000

Related Devices (Code: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, Inc.

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.

↑