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FDA 510(k)

MODIFIED CASTLE POWERCLAVE

K-Number: K870975 · 1987-04-17

ApplicantCastle Co.
Decision Date1987-04-17
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED CASTLE POWERCLAVE is the device name listed in this FDA 510(k) record. The listed applicant is Castle Co.. It received FDA 510(k) clearance on 1987-04-17 under 510(k) number K870975. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CASTLE POWERCLAVE?

MODIFIED CASTLE POWERCLAVE is a medical device that received FDA 510(k) clearance on 1987-04-17. The listed applicant is Castle Co.. The 510(k) number is K870975.

When did MODIFIED CASTLE POWERCLAVE receive FDA 510(k) clearance?

MODIFIED CASTLE POWERCLAVE received FDA 510(k) clearance on 1987-04-17, under 510(k) number K870975.

Who is the listed applicant for MODIFIED CASTLE POWERCLAVE?

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

What is the FDA product code for MODIFIED CASTLE POWERCLAVE?

The FDA product code for MODIFIED CASTLE POWERCLAVE is FLE.

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Other records listing Castle Co. 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.

K860263CASTLE 7538 FLOOR LOADING WASHERK844089CASTLE 7515 UTENSIL/GLASSWARE WASHERK834048BOVIE CONDUCTIVE ADHES-DISPER-ELECTROK833074CASTLE TEC-TEST S.M.A.R.T. PACKK831595CASTLE MODEL 3341 & 3441 & 4141 GAS AERK792649UNISPORE-BIOLOGICAL INDICATORS

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Related Devices (Code: FLE)

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.

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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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