BLOOD COLLECTION SET TYPE H
K-Number: K771269 · 1977-09-12
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Device Summary
Frequently Asked Questions
What is the BLOOD COLLECTION SET TYPE H?
BLOOD COLLECTION SET TYPE H 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 K771269.
When did BLOOD COLLECTION SET TYPE H receive FDA 510(k) clearance?
BLOOD COLLECTION SET TYPE H received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771269.
Who is the listed applicant for BLOOD COLLECTION SET TYPE H?
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 BLOOD COLLECTION SET TYPE H?
The FDA product code for BLOOD COLLECTION SET TYPE H is FPK.
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: FPK)
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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