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)

DOUCHE KIT, SOMETHING PERSONAL

K-Number: K781207 · 1978-08-10

ApplicantChatten Drug & Chemical Co.
Decision Date1978-08-10
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUCHE KIT, SOMETHING PERSONAL is the device name listed in this FDA 510(k) record. The listed applicant is Chatten Drug & Chemical Co.. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K781207. The device is classified under product code HED. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUCHE KIT, SOMETHING PERSONAL?

DOUCHE KIT, SOMETHING PERSONAL is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Chatten Drug & Chemical Co.. The 510(k) number is K781207.

When did DOUCHE KIT, SOMETHING PERSONAL receive FDA 510(k) clearance?

DOUCHE KIT, SOMETHING PERSONAL received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781207.

Who is the listed applicant for DOUCHE KIT, SOMETHING PERSONAL?

The FDA 510(k) record lists Chatten Drug & Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOUCHE KIT, SOMETHING PERSONAL?

The FDA product code for DOUCHE KIT, SOMETHING PERSONAL is HED.

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: HED)

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.

K080200WATER WORKS DOUCHING DEVICEAbbott Research Group, Inc.K030056WORRY-REMOVER IRRIGATORCorisen Group, Ltd.K000736LA JOIEGoomi Ehwa, Inc.K902830PERI-BOTTLEOrion Life Systems, Inc.K881216GENT-L-KARE VAGINAL IRRIGATION SETGeneva Laboratories, Inc.K854595P.A. MEDICAL VAGINAL IRRIGATION SET #1130Pa Medical Corp.

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.

↑