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FDA 510(k)

CONVERTORS FLASH STERILIZING TRAY

K-Number: K832137 · 1983-08-12

Decision Date1983-08-12
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONVERTORS FLASH STERILIZING TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Convertors Div., American Pharmaseal. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832137. 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 CONVERTORS FLASH STERILIZING TRAY?

CONVERTORS FLASH STERILIZING TRAY is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is American Convertors Div., American Pharmaseal. The 510(k) number is K832137.

When did CONVERTORS FLASH STERILIZING TRAY receive FDA 510(k) clearance?

CONVERTORS FLASH STERILIZING TRAY received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832137.

Who is the listed applicant for CONVERTORS FLASH STERILIZING TRAY?

The FDA 510(k) record lists American Convertors Div., American Pharmaseal as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVERTORS FLASH STERILIZING TRAY?

The FDA product code for CONVERTORS FLASH STERILIZING 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 American Convertors Div., American Pharmaseal 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 19 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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