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FDA 510(k)

PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS

K-Number: K871132 · 1987-04-20

Decision Date1987-04-20
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS is the device name listed in this FDA 510(k) record. The listed applicant is Deltec Systems, Inc.. It received FDA 510(k) clearance on 1987-04-20 under 510(k) number K871132. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS?

PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS is a medical device that received FDA 510(k) clearance on 1987-04-20. The listed applicant is Deltec Systems, Inc.. The 510(k) number is K871132.

When did PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS receive FDA 510(k) clearance?

PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS received FDA 510(k) clearance on 1987-04-20, under 510(k) number K871132.

Who is the listed applicant for PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS?

The FDA 510(k) record lists Deltec Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS?

The FDA product code for PHARMACIA DELTEC SUBCLAVIAN INTRODUCERS is DYB.

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 Deltec Systems, 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.

View all 9 devices →

Related Devices (Code: DYB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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