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FDA 510(k)

HAMACHER BULLET POINT OPHTHALMIC NEEDLE

K-Number: K872200 · 1987-06-25

ApplicantR. J. Doyle, Inc.
Decision Date1987-06-25
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HAMACHER BULLET POINT OPHTHALMIC NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is R. J. Doyle, Inc.. It received FDA 510(k) clearance on 1987-06-25 under 510(k) number K872200. 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 HAMACHER BULLET POINT OPHTHALMIC NEEDLE?

HAMACHER BULLET POINT OPHTHALMIC NEEDLE is a medical device that received FDA 510(k) clearance on 1987-06-25. The listed applicant is R. J. Doyle, Inc.. The 510(k) number is K872200.

When did HAMACHER BULLET POINT OPHTHALMIC NEEDLE receive FDA 510(k) clearance?

HAMACHER BULLET POINT OPHTHALMIC NEEDLE received FDA 510(k) clearance on 1987-06-25, under 510(k) number K872200.

Who is the listed applicant for HAMACHER BULLET POINT OPHTHALMIC NEEDLE?

The FDA 510(k) record lists R. J. Doyle, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAMACHER BULLET POINT OPHTHALMIC NEEDLE?

The FDA product code for HAMACHER BULLET POINT OPHTHALMIC NEEDLE 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 R. J. Doyle, 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.

K89488120GA X 7-1/2 THREADING BULLET POINT NEEDLEK89488016GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDLK894882INFILTRATION PUMP SYRINGEK89487916GA X 10 MIDDLE SIZE BULLET POINT NEEDLEK89487816GA X 6 BULLET POINT NEEDLE, FLEX STAINLESS STEEK89487520GA X 7-1/2 THREADING BULLET POINT NEEDLE

View all 10 devices →

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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