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FDA 510(k)

CURITY 100% SILICONE SAFETY INDICATOR

K-Number: K810690 · 1981-04-23

ApplicantThe Kendal Co.
Decision Date1981-04-23
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CURITY 100% SILICONE SAFETY INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810690. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY 100% SILICONE SAFETY INDICATOR?

CURITY 100% SILICONE SAFETY INDICATOR is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is The Kendal Co.. The 510(k) number is K810690.

When did CURITY 100% SILICONE SAFETY INDICATOR receive FDA 510(k) clearance?

CURITY 100% SILICONE SAFETY INDICATOR received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810690.

Who is the listed applicant for CURITY 100% SILICONE SAFETY INDICATOR?

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

What is the FDA product code for CURITY 100% SILICONE SAFETY INDICATOR?

The FDA product code for CURITY 100% SILICONE SAFETY INDICATOR is KOD.

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Other records listing The Kendal Co. as applicant

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Related Devices (Code: KOD)

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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