INFUSION SET TYPE S
K-Number: K771267 · 1977-09-12
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Device Summary
Frequently Asked Questions
What is the INFUSION SET TYPE S?
INFUSION SET TYPE S is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Berman, Pcp & Consultants, Inc.. The 510(k) number is K771267.
When did INFUSION SET TYPE S receive FDA 510(k) clearance?
INFUSION SET TYPE S received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771267.
Who is the listed applicant for INFUSION SET TYPE S?
The FDA 510(k) record lists Berman, Pcp & Consultants, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION SET TYPE S?
The FDA product code for INFUSION SET TYPE S is FPA.
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 Berman, Pcp & Consultants, 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: FPA)
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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