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FDA 510(k)

LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH

K-Number: K872884 · 1987-08-10

ApplicantLook, Inc.
Decision Date1987-08-10
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K872884. 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 IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH?

LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Look, Inc.. The 510(k) number is K872884.

When did LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH receive FDA 510(k) clearance?

LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH received FDA 510(k) clearance on 1987-08-10, under 510(k) number K872884.

Who is the listed applicant for LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH?

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 IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH?

The FDA product code for LOOK IRRIGATING/ASPIRATING CANNULA W/TEFLON SHEATH 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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