PM 25 PP (BODY AID)
K-Number: K780914 · 1978-06-14
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Device Summary
Frequently Asked Questions
What is the PM 25 PP (BODY AID)?
PM 25 PP (BODY AID) is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Argosy Intl. (Usa), Inc.. The 510(k) number is K780914.
When did PM 25 PP (BODY AID) receive FDA 510(k) clearance?
PM 25 PP (BODY AID) received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780914.
Who is the listed applicant for PM 25 PP (BODY AID)?
The FDA 510(k) record lists Argosy Intl. (Usa), Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PM 25 PP (BODY AID)?
The FDA product code for PM 25 PP (BODY AID) is ESD.
Other records listing Argosy Intl. (Usa), 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: ESD)
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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