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FDA 510(k)

INFUSION CANNULAM

K-Number: K852758 · 1985-08-01

ApplicantPrecision Medical Instruments, Inc.
Decision Date1985-08-01
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INFUSION CANNULAM is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical Instruments, Inc.. It received FDA 510(k) clearance on 1985-08-01 under 510(k) number K852758. 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 INFUSION CANNULAM?

INFUSION CANNULAM is a medical device that received FDA 510(k) clearance on 1985-08-01. The listed applicant is Precision Medical Instruments, Inc.. The 510(k) number is K852758.

When did INFUSION CANNULAM receive FDA 510(k) clearance?

INFUSION CANNULAM received FDA 510(k) clearance on 1985-08-01, under 510(k) number K852758.

Who is the listed applicant for INFUSION CANNULAM?

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

What is the FDA product code for INFUSION CANNULAM?

The FDA product code for INFUSION CANNULAM 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 Precision Medical Instruments, 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.

K832560ASPIRATING HANDLE W/BACKFLUSHING CAPABK830037EXTENSION HANDLE FOR ACUTOME PROBEK791212VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG

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

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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