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FDA 510(k)

GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR

K-Number: K844613 · 1985-01-10

Decision Date1985-01-10
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR 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 1985-01-10 under 510(k) number K844613. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR?

GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR is a medical device that received FDA 510(k) clearance on 1985-01-10. The listed applicant is Packaging Technologies, Inc.. The 510(k) number is K844613.

When did GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR receive FDA 510(k) clearance?

GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR received FDA 510(k) clearance on 1985-01-10, under 510(k) number K844613.

Who is the listed applicant for GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR?

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 GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR?

The FDA product code for GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR is FSM.

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: FSM)

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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