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FDA 510(k)

MOBAY (BAYER) MERLON M-40 (H)F 1112

K-Number: K873822 · 1988-03-24

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

Device Summary

MOBAY (BAYER) MERLON M-40 (H)F 1112 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 K873822. 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) MERLON M-40 (H)F 1112?

MOBAY (BAYER) MERLON M-40 (H)F 1112 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 K873822.

When did MOBAY (BAYER) MERLON M-40 (H)F 1112 receive FDA 510(k) clearance?

MOBAY (BAYER) MERLON M-40 (H)F 1112 received FDA 510(k) clearance on 1988-03-24, under 510(k) number K873822.

Who is the listed applicant for MOBAY (BAYER) MERLON M-40 (H)F 1112?

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) MERLON M-40 (H)F 1112?

The FDA product code for MOBAY (BAYER) MERLON M-40 (H)F 1112 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 1112K873823MOBAY (BAYER) MAKROLON 2658 3291K871714KESTREL 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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