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FDA 510(k)

PORCELIT

K-Number: K790806 · 1979-08-03

ApplicantHarry J. Bosworth Co.
Decision Date1979-08-03
Product CodeEBA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORCELIT is the device name listed in this FDA 510(k) record. The listed applicant is Harry J. Bosworth Co.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K790806. The device is classified under product code EBA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORCELIT?

PORCELIT is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K790806.

When did PORCELIT receive FDA 510(k) clearance?

PORCELIT received FDA 510(k) clearance on 1979-08-03, under 510(k) number K790806.

Who is the listed applicant for PORCELIT?

The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORCELIT?

The FDA product code for PORCELIT is EBA.

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Other records listing Harry J. Bosworth Co. as applicant

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Related Devices (Code: EBA)

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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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