PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET
K-Number: K873885 · 1987-11-03
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Device Summary
Frequently Asked Questions
What is the PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET?
PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET is a medical device that received FDA 510(k) clearance on 1987-11-03. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K873885.
When did PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET receive FDA 510(k) clearance?
PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET received FDA 510(k) clearance on 1987-11-03, under 510(k) number K873885.
Who is the listed applicant for PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET?
The FDA 510(k) record lists Pharmacia Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET?
The FDA product code for PHARMACIA DELTEC SUBCUTANEOUS INFUSION SET 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 Pharmacia Deltec, 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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