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)

REYNOLDS BLEACHING PROCESS

K-Number: K790378 · 1979-04-10

ApplicantReynolds Laboratories
Decision Date1979-04-10
Product CodeEEG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REYNOLDS BLEACHING PROCESS is the device name listed in this FDA 510(k) record. The listed applicant is Reynolds Laboratories. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790378. The device is classified under product code EEG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REYNOLDS BLEACHING PROCESS?

REYNOLDS BLEACHING PROCESS is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Reynolds Laboratories. The 510(k) number is K790378.

When did REYNOLDS BLEACHING PROCESS receive FDA 510(k) clearance?

REYNOLDS BLEACHING PROCESS received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790378.

Who is the listed applicant for REYNOLDS BLEACHING PROCESS?

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

What is the FDA product code for REYNOLDS BLEACHING PROCESS?

The FDA product code for REYNOLDS BLEACHING PROCESS is EEG.

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

Related Devices (Code: EEG)

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.

K122725TANDA PEARL, ULTRAWYTE, PEARLSyneron BeautyK110888ABSOLUTE WHITE LIGHTDr. Fresh, Inc.K063704BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW1101Beks IncorporatedK052040QUICKSMILECosmetic Dental Materials, Inc.K041392SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE USCAO Group, Inc.K042153SOUTH BEACH SMILE LIGHT WHITENING SYSTEMDentovations, 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.

↑