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FDA 510(k)

RICHARD-ALLAN SHEET CLIP

K-Number: K905701 · 1991-02-19

ApplicantRichard-Allan Medical
Decision Date1991-02-19
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RICHARD-ALLAN SHEET CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical. It received FDA 510(k) clearance on 1991-02-19 under 510(k) number K905701. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICHARD-ALLAN SHEET CLIP?

RICHARD-ALLAN SHEET CLIP is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Richard-Allan Medical. The 510(k) number is K905701.

When did RICHARD-ALLAN SHEET CLIP receive FDA 510(k) clearance?

RICHARD-ALLAN SHEET CLIP received FDA 510(k) clearance on 1991-02-19, under 510(k) number K905701.

Who is the listed applicant for RICHARD-ALLAN SHEET CLIP?

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

What is the FDA product code for RICHARD-ALLAN SHEET CLIP?

The FDA product code for RICHARD-ALLAN SHEET CLIP is KKX.

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Other records listing Richard-Allan Medical 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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