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)

CONVERSION CONTRACTOR TIMER KIT

K-Number: K791933 · 1979-11-13

ApplicantAdvanced Instrument Development, Inc.
Decision Date1979-11-13
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONVERSION CONTRACTOR TIMER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instrument Development, Inc.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K791933. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERSION CONTRACTOR TIMER KIT?

CONVERSION CONTRACTOR TIMER KIT is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Advanced Instrument Development, Inc.. The 510(k) number is K791933.

When did CONVERSION CONTRACTOR TIMER KIT receive FDA 510(k) clearance?

CONVERSION CONTRACTOR TIMER KIT received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791933.

Who is the listed applicant for CONVERSION CONTRACTOR TIMER KIT?

The FDA 510(k) record lists Advanced Instrument Development, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVERSION CONTRACTOR TIMER KIT?

The FDA product code for CONVERSION CONTRACTOR TIMER KIT is IZO.

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 Advanced Instrument Development, Inc. 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.

K974863IMIX DIGITAL THORAX SYSTEMK872445POWER-AID INDEPENDENT X-RAY POWER SOURCEK827525AUTOMATIC EXPOSURE CONTROL TYPE A3300K813128MOBIL-AID AUTOMATIC EXPOSURE CONTROL

Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, 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.

↑