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FDA 510(k)

MICROINFERTILITY NEEDLE HOLDER, TITANIUM

K-Number: K844821 · 1985-01-16

Decision Date1985-01-16
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MICROINFERTILITY NEEDLE HOLDER, TITANIUM is the device name listed in this FDA 510(k) record. The listed applicant is Precision Surgical Instrument, Inc.. It received FDA 510(k) clearance on 1985-01-16 under 510(k) number K844821. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROINFERTILITY NEEDLE HOLDER, TITANIUM?

MICROINFERTILITY NEEDLE HOLDER, TITANIUM is a medical device that received FDA 510(k) clearance on 1985-01-16. The listed applicant is Precision Surgical Instrument, Inc.. The 510(k) number is K844821.

When did MICROINFERTILITY NEEDLE HOLDER, TITANIUM receive FDA 510(k) clearance?

MICROINFERTILITY NEEDLE HOLDER, TITANIUM received FDA 510(k) clearance on 1985-01-16, under 510(k) number K844821.

Who is the listed applicant for MICROINFERTILITY NEEDLE HOLDER, TITANIUM?

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

What is the FDA product code for MICROINFERTILITY NEEDLE HOLDER, TITANIUM?

The FDA product code for MICROINFERTILITY NEEDLE HOLDER, TITANIUM is KNA.

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.

Other records listing Precision Surgical Instrument, 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.

Related Devices (Code: KNA)

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.

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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