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FDA 510(k)

CAL-RITE

K-Number: K811801 · 1981-07-28

Decision Date1981-07-28
Product CodeKDX
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CAL-RITE is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811801. The device is classified under product code KDX. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAL-RITE?

CAL-RITE is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K811801.

When did CAL-RITE receive FDA 510(k) clearance?

CAL-RITE received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811801.

Who is the listed applicant for CAL-RITE?

The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAL-RITE?

The FDA product code for CAL-RITE is KDX.

Other records listing Richard-Allan Medical Ind., Inc. 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 33 devices →

Related Devices (Code: KDX)

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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