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FDA 510(k)

LOOK IRRIGATING CANNULAS

K-Number: K870438 · 1987-02-20

ApplicantLook, Inc.
Decision Date1987-02-20
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOOK IRRIGATING CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870438. 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 CANNULAS?

LOOK IRRIGATING CANNULAS is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Look, Inc.. The 510(k) number is K870438.

When did LOOK IRRIGATING CANNULAS receive FDA 510(k) clearance?

LOOK IRRIGATING CANNULAS received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870438.

Who is the listed applicant for LOOK IRRIGATING CANNULAS?

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 CANNULAS?

The FDA product code for LOOK IRRIGATING CANNULAS 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.

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.

View all 25 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.

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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