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FDA 510(k)

CASTLE TEC-TEST BIOLOGICAL INDICATOR

K-Number: K812272 · 1981-09-08

ApplicantSybron Corp.
Decision Date1981-09-08
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CASTLE TEC-TEST BIOLOGICAL INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K812272. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASTLE TEC-TEST BIOLOGICAL INDICATOR?

CASTLE TEC-TEST BIOLOGICAL INDICATOR is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Sybron Corp.. The 510(k) number is K812272.

When did CASTLE TEC-TEST BIOLOGICAL INDICATOR receive FDA 510(k) clearance?

CASTLE TEC-TEST BIOLOGICAL INDICATOR received FDA 510(k) clearance on 1981-09-08, under 510(k) number K812272.

Who is the listed applicant for CASTLE TEC-TEST BIOLOGICAL INDICATOR?

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

What is the FDA product code for CASTLE TEC-TEST BIOLOGICAL INDICATOR?

The FDA product code for CASTLE TEC-TEST BIOLOGICAL INDICATOR is FRC.

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Other records listing Sybron Corp. as applicant

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Related Devices (Code: FRC)

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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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