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FDA 510(k)

PROTECTOR II

K-Number: K790661 · 1979-04-12

ApplicantRichard-Allan Medical Ind., Inc.
Decision Date1979-04-12
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROTECTOR II 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 1979-04-12 under 510(k) number K790661. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTECTOR II?

PROTECTOR II is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K790661.

When did PROTECTOR II receive FDA 510(k) clearance?

PROTECTOR II received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790661.

Who is the listed applicant for PROTECTOR II?

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 PROTECTOR II?

The FDA product code for PROTECTOR II is MMK.

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Other records listing Richard-Allan Medical Ind., Inc. as applicant

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Related Devices (Code: MMK)

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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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