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FDA 510(k)

MOBAY (BAYER) MAKROLON 2658 3291

K-Number: K873823 · 1988-03-24

ApplicantApplied Laboratories, Inc.
Decision Date1988-03-24
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MOBAY (BAYER) MAKROLON 2658 3291 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Laboratories, Inc.. It received FDA 510(k) clearance on 1988-03-24 under 510(k) number K873823. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBAY (BAYER) MAKROLON 2658 3291?

MOBAY (BAYER) MAKROLON 2658 3291 is a medical device that received FDA 510(k) clearance on 1988-03-24. The listed applicant is Applied Laboratories, Inc.. The 510(k) number is K873823.

When did MOBAY (BAYER) MAKROLON 2658 3291 receive FDA 510(k) clearance?

MOBAY (BAYER) MAKROLON 2658 3291 received FDA 510(k) clearance on 1988-03-24, under 510(k) number K873823.

Who is the listed applicant for MOBAY (BAYER) MAKROLON 2658 3291?

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

What is the FDA product code for MOBAY (BAYER) MAKROLON 2658 3291?

The FDA product code for MOBAY (BAYER) MAKROLON 2658 3291 is LRX.

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Other records listing Applied Laboratories, 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.

K873824RED #467, #457, BLUE #437, GREEN #447 MINDEL S1000K873825GE LEXAN 144R 112K873821GE NORYL 731-80089SK873820MOBAY (BAYER) MAKROLON 2658 1112K873822MOBAY (BAYER) MERLON M-40 (H)F 1112K871714KESTREL CONTACT LENS CASE

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Related Devices (Code: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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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