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FDA 510(k)

MEMORY STAPLE (20 SIZES AVAILABLE)

K-Number: K964226 · 1997-08-05

ApplicantLandos, Inc.
Decision Date1997-08-05
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMORY STAPLE (20 SIZES AVAILABLE) is the device name listed in this FDA 510(k) record. The listed applicant is Landos, Inc.. It received FDA 510(k) clearance on 1997-08-05 under 510(k) number K964226. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMORY STAPLE (20 SIZES AVAILABLE)?

MEMORY STAPLE (20 SIZES AVAILABLE) is a medical device that received FDA 510(k) clearance on 1997-08-05. The listed applicant is Landos, Inc.. The 510(k) number is K964226.

When did MEMORY STAPLE (20 SIZES AVAILABLE) receive FDA 510(k) clearance?

MEMORY STAPLE (20 SIZES AVAILABLE) received FDA 510(k) clearance on 1997-08-05, under 510(k) number K964226.

Who is the listed applicant for MEMORY STAPLE (20 SIZES AVAILABLE)?

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

What is the FDA product code for MEMORY STAPLE (20 SIZES AVAILABLE)?

The FDA product code for MEMORY STAPLE (20 SIZES AVAILABLE) is JDR.

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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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