PERIODONTIC TOOTHBRUSH, #0126-0190-00
K-Number: K771185 · 1977-07-15
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Device Summary
Frequently Asked Questions
What is the PERIODONTIC TOOTHBRUSH, #0126-0190-00?
PERIODONTIC TOOTHBRUSH, #0126-0190-00 is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Hoyt Laboratories. The 510(k) number is K771185.
When did PERIODONTIC TOOTHBRUSH, #0126-0190-00 receive FDA 510(k) clearance?
PERIODONTIC TOOTHBRUSH, #0126-0190-00 received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771185.
Who is the listed applicant for PERIODONTIC TOOTHBRUSH, #0126-0190-00?
The FDA 510(k) record lists Hoyt Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERIODONTIC TOOTHBRUSH, #0126-0190-00?
The FDA product code for PERIODONTIC TOOTHBRUSH, #0126-0190-00 is EFW.
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 Hoyt Laboratories 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: EFW)
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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