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FDA 510(k)

WOUND CLOSURE INSTRUMENT TRAY

K-Number: K812133 · 1982-01-08

ApplicantE.M. Adams
Decision Date1982-01-08
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WOUND CLOSURE INSTRUMENT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1982-01-08 under 510(k) number K812133. 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 WOUND CLOSURE INSTRUMENT TRAY?

WOUND CLOSURE INSTRUMENT TRAY is a medical device that received FDA 510(k) clearance on 1982-01-08. The listed applicant is E.M. Adams. The 510(k) number is K812133.

When did WOUND CLOSURE INSTRUMENT TRAY receive FDA 510(k) clearance?

WOUND CLOSURE INSTRUMENT TRAY received FDA 510(k) clearance on 1982-01-08, under 510(k) number K812133.

Who is the listed applicant for WOUND CLOSURE INSTRUMENT TRAY?

The FDA 510(k) record lists E.M. Adams as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WOUND CLOSURE INSTRUMENT TRAY?

The FDA product code for WOUND CLOSURE INSTRUMENT TRAY 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 E.M. Adams 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 21 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

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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