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FDA 510(k)

LOOK RETROBULBAR NEEDLES

K-Number: K870902 · 1987-03-20

ApplicantLook, Inc.
Decision Date1987-03-20
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOOK RETROBULBAR NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K870902. 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 LOOK RETROBULBAR NEEDLES?

LOOK RETROBULBAR NEEDLES is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Look, Inc.. The 510(k) number is K870902.

When did LOOK RETROBULBAR NEEDLES receive FDA 510(k) clearance?

LOOK RETROBULBAR NEEDLES received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870902.

Who is the listed applicant for LOOK RETROBULBAR NEEDLES?

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

What is the FDA product code for LOOK RETROBULBAR NEEDLES?

The FDA product code for LOOK RETROBULBAR NEEDLES is HMX.

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Other records listing Look, 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.

K943949POLYVIOLENE SURGICL SUTUREK933686LOOK INC. 316L STAINLESS STEEL SURGICAL SUTUREK926586REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURESK926587REVISED LABELING FOR NYLON SUTURE (POLYAMIDE)K926167POLYVIOLENE SUTURE-REVISED LABELINGK926168SILK SUTURES-REVISED LABELING

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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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