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FDA 510(k)

SINGLE BASIN SET

K-Number: K844611 · 1984-12-19

Decision Date1984-12-19
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SINGLE BASIN SET is the device name listed in this FDA 510(k) record. The listed applicant is Packaging Technologies, Inc.. It received FDA 510(k) clearance on 1984-12-19 under 510(k) number K844611. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE BASIN SET?

SINGLE BASIN SET is a medical device that received FDA 510(k) clearance on 1984-12-19. The listed applicant is Packaging Technologies, Inc.. The 510(k) number is K844611.

When did SINGLE BASIN SET receive FDA 510(k) clearance?

SINGLE BASIN SET received FDA 510(k) clearance on 1984-12-19, under 510(k) number K844611.

Who is the listed applicant for SINGLE BASIN SET?

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

What is the FDA product code for SINGLE BASIN SET?

The FDA product code for SINGLE BASIN SET is FRG.

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 Packaging Technologies, 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 13 devices →

Related Devices (Code: FRG)

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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