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FDA 510(k)

NLD IMPLANT SET

K-Number: K813314 · 1982-02-24

ApplicantDesign Research Assoc., Inc.
Decision Date1982-02-24
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NLD IMPLANT SET is the device name listed in this FDA 510(k) record. The listed applicant is Design Research Assoc., Inc.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K813314. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NLD IMPLANT SET?

NLD IMPLANT SET is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Design Research Assoc., Inc.. The 510(k) number is K813314.

When did NLD IMPLANT SET receive FDA 510(k) clearance?

NLD IMPLANT SET received FDA 510(k) clearance on 1982-02-24, under 510(k) number K813314.

Who is the listed applicant for NLD IMPLANT SET?

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

What is the FDA product code for NLD IMPLANT SET?

The FDA product code for NLD IMPLANT SET is HMX.

Related Clinical Trials

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.

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Other records listing Design Research Assoc., 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.

K813313BIOMICROSCOPY CONTACT LENSK813315CALIPER-OPTHALMIC

Related Devices (Code: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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