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FDA 510(k)

NEEDLE GUIDE MODEL 21285A

K-Number: K830753 · 1983-06-16

ApplicantHewlett-Packard Co.
Decision Date1983-06-16
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

NEEDLE GUIDE MODEL 21285A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1983-06-16 under 510(k) number K830753. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE GUIDE MODEL 21285A?

NEEDLE GUIDE MODEL 21285A is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K830753.

When did NEEDLE GUIDE MODEL 21285A receive FDA 510(k) clearance?

NEEDLE GUIDE MODEL 21285A received FDA 510(k) clearance on 1983-06-16, under 510(k) number K830753.

Who is the listed applicant for NEEDLE GUIDE MODEL 21285A?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE GUIDE MODEL 21285A?

The FDA product code for NEEDLE GUIDE MODEL 21285A is LFL.

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Related Devices (Code: LFL)

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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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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