ADAPTER, PER-CEN-TOX-BODY
K-Number: K760518 · 1976-09-03
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Device Summary
Frequently Asked Questions
What is the ADAPTER, PER-CEN-TOX-BODY?
ADAPTER, PER-CEN-TOX-BODY is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Landmark Plastics. The 510(k) number is K760518.
When did ADAPTER, PER-CEN-TOX-BODY receive FDA 510(k) clearance?
ADAPTER, PER-CEN-TOX-BODY received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760518.
Who is the listed applicant for ADAPTER, PER-CEN-TOX-BODY?
The FDA 510(k) record lists Landmark Plastics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADAPTER, PER-CEN-TOX-BODY?
The FDA product code for ADAPTER, PER-CEN-TOX-BODY is BYF.
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 Landmark Plastics 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: BYF)
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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