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FDA 510(k)

TRACHEOSTOMY CARE TRAYS

K-Number: K832880 · 1983-10-31

Decision Date1983-10-31
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRACHEOSTOMY CARE TRAYS 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 1983-10-31 under 510(k) number K832880. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACHEOSTOMY CARE TRAYS?

TRACHEOSTOMY CARE TRAYS is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Packaging Technologies, Inc.. The 510(k) number is K832880.

When did TRACHEOSTOMY CARE TRAYS receive FDA 510(k) clearance?

TRACHEOSTOMY CARE TRAYS received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832880.

Who is the listed applicant for TRACHEOSTOMY CARE TRAYS?

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 TRACHEOSTOMY CARE TRAYS?

The FDA product code for TRACHEOSTOMY CARE TRAYS is JOL.

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: JOL)

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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