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FDA 510(k)

PROTECTOR (SURGICAL INSTRUMENT)

K-Number: K890314 · 1989-02-27

ApplicantRichard-Allan Medical Ind., Inc.
Decision Date1989-02-27
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROTECTOR (SURGICAL INSTRUMENT) 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 1989-02-27 under 510(k) number K890314. 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 (SURGICAL INSTRUMENT)?

PROTECTOR (SURGICAL INSTRUMENT) is a medical device that received FDA 510(k) clearance on 1989-02-27. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K890314.

When did PROTECTOR (SURGICAL INSTRUMENT) receive FDA 510(k) clearance?

PROTECTOR (SURGICAL INSTRUMENT) received FDA 510(k) clearance on 1989-02-27, under 510(k) number K890314.

Who is the listed applicant for PROTECTOR (SURGICAL INSTRUMENT)?

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 (SURGICAL INSTRUMENT)?

The FDA product code for PROTECTOR (SURGICAL INSTRUMENT) is MMK.

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

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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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