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FDA 510(k)

MODEL 1330 EXTENSION SET

K-Number: K873042 · 1987-10-23

Decision Date1987-10-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 1330 EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K873042. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1330 EXTENSION SET?

MODEL 1330 EXTENSION SET is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K873042.

When did MODEL 1330 EXTENSION SET receive FDA 510(k) clearance?

MODEL 1330 EXTENSION SET received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873042.

Who is the listed applicant for MODEL 1330 EXTENSION 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 MODEL 1330 EXTENSION SET?

The FDA product code for MODEL 1330 EXTENSION 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.

View all 43 devices →

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

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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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