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FDA 510(k)

MICROSPEARS

K-Number: K780257 · 1978-02-23

ApplicantSparta Instrument Corp.
Decision Date1978-02-23
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICROSPEARS is the device name listed in this FDA 510(k) record. The listed applicant is Sparta Instrument Corp.. It received FDA 510(k) clearance on 1978-02-23 under 510(k) number K780257. The device is classified under product code HOZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSPEARS?

MICROSPEARS is a medical device that received FDA 510(k) clearance on 1978-02-23. The listed applicant is Sparta Instrument Corp.. The 510(k) number is K780257.

When did MICROSPEARS receive FDA 510(k) clearance?

MICROSPEARS received FDA 510(k) clearance on 1978-02-23, under 510(k) number K780257.

Who is the listed applicant for MICROSPEARS?

The FDA 510(k) record lists Sparta Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSPEARS?

The FDA product code for MICROSPEARS is HOZ.

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 Sparta Instrument Corp. 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.

K854475GHAJAR INTRAVENTRICULAR CATHETER GUIDEK781365SPARTA BRONCHIAL BRUSHK780258MILK BATH CONCENTRATE

Related Devices (Code: HOZ)

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.

K132796SUNTOUCH EYE SPEARHuizhou Foryou Medical Devices Co., Ltd.K130117NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDSNetwork Medical Products, Ltd.K091240ALPHAMED SURGICAL SPEAR, MODEL 70-5000Alphamed, Inc.K082460CENEFOM PVA SURGICAL SPEARLongtek Scientific Co., Ltd.K012196ULTRACELL ABSORBENT STICKUltracell Medical Technologies, Inc.K011191MEROCEL CORNELL LID AND LASH GUARD, MEROCEL AND KEROCEL OPHTHALMIC SPONGESMedtronic Xomed, 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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