ENEMA CONTAINER DISP. FOR EMEMA ADMIN.
K-Number: K800961 · 1980-05-14
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Device Summary
Frequently Asked Questions
What is the ENEMA CONTAINER DISP. FOR EMEMA ADMIN.?
ENEMA CONTAINER DISP. FOR EMEMA ADMIN. is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K800961.
When did ENEMA CONTAINER DISP. FOR EMEMA ADMIN. receive FDA 510(k) clearance?
ENEMA CONTAINER DISP. FOR EMEMA ADMIN. received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800961.
Who is the listed applicant for ENEMA CONTAINER DISP. FOR EMEMA ADMIN.?
The FDA 510(k) record lists The Healthcare Group Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENEMA CONTAINER DISP. FOR EMEMA ADMIN.?
The FDA product code for ENEMA CONTAINER DISP. FOR EMEMA ADMIN. is FCE.
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 Healthcare Group Laboratories, 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.
Related Devices (Code: FCE)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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