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FDA 510(k)

LOOK VISCODISSECTOR

K-Number: K913530 · 1991-10-21

ApplicantLook, Inc.
Decision Date1991-10-21
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOOK VISCODISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1991-10-21 under 510(k) number K913530. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOOK VISCODISSECTOR?

LOOK VISCODISSECTOR is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Look, Inc.. The 510(k) number is K913530.

When did LOOK VISCODISSECTOR receive FDA 510(k) clearance?

LOOK VISCODISSECTOR received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913530.

Who is the listed applicant for LOOK VISCODISSECTOR?

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 VISCODISSECTOR?

The FDA product code for LOOK VISCODISSECTOR is HQC.

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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 SUTURESK926167POLYVIOLENE SUTURE-REVISED LABELINGK926587REVISED LABELING FOR NYLON SUTURE (POLYAMIDE)K926168SILK SUTURES-REVISED LABELING

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Related Devices (Code: HQC)

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.

K261264Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+Bausch and LombK252052Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)Bausch and Lomb, IncorporatedK250501System SophiThis AGK243395MICOR 700 with Auto I/ACarl Zeiss Meditec Cataract Technology, Inc.K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)Carl Zeiss Meditec Cataract Technology, Inc.K240169Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)Bausch and Lomb, Incorporated

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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