FDA 510(k)

LID LOC

K-Number: K895364 · 1989-10-31

Decision Date1989-10-31

Product CodeHOY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

LID LOC is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum Co.. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K895364. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LID LOC?

LID LOC is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is Spectrum Co.. The 510(k) number is K895364.

When did LID LOC receive FDA 510(k) clearance?

LID LOC received FDA 510(k) clearance on 1989-10-31, under 510(k) number K895364.

Who is the listed applicant for LID LOC?

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

What is the FDA product code for LID LOC?

The FDA product code for LID LOC is HOY.

Other records listing Spectrum Co. 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.

K874604HISTOBRUSH K823179CHLAMYDIA TRANSETTEE 1 & 3

Related Devices (Code: HOY)

K050856LCG (LIQUIDE CRYSTAL GLASSES) SYSTEMOphthocare , Ltd.K971465NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYSNational Healthcare Mfg. Corp.K944700ARCTIC PREMIER SERIESSungold Eyewear, Inc.K944857GOGGLE SAFEGUARDSellstrom Mfg. Co.K945351SHIELD, EYE, OPHTHALMICTaiwan Eva Industrial Co., Inc.K945346MAKROLON 2405 GOGGLES (LIGHT AND DARK)Universal Massage & Tanning, 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.