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FDA 510(k)

MINOR LAP SET

K-Number: K921732 · 1994-06-15

ApplicantMedikmark, Inc.
Decision Date1994-06-15
Product CodeKOH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINOR LAP SET is the device name listed in this FDA 510(k) record. The listed applicant is Medikmark, Inc.. It received FDA 510(k) clearance on 1994-06-15 under 510(k) number K921732. The device is classified under product code KOH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINOR LAP SET?

MINOR LAP SET is a medical device that received FDA 510(k) clearance on 1994-06-15. The listed applicant is Medikmark, Inc.. The 510(k) number is K921732.

When did MINOR LAP SET receive FDA 510(k) clearance?

MINOR LAP SET received FDA 510(k) clearance on 1994-06-15, under 510(k) number K921732.

Who is the listed applicant for MINOR LAP SET?

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

What is the FDA product code for MINOR LAP SET?

The FDA product code for MINOR LAP SET is KOH.

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Other records listing Medikmark, 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.

K953474IV START KITK923960UPPER EXTERMITY DRAPE KITK921733TRACHEOSTOMY CARE TRAYK921730C-SECTION PACKK920341LACERATION TRAYSK920340SUTURE REMOVAL KIT

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Related Devices (Code: KOH)

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.

K000212KSEA CHARDONNES MORCELLATION KNIFEKARL STORZ Endoscopy-America, Inc.K921730C-SECTION PACKMedikmark, Inc.K891351NEWPORT LATERAL VAGINAL RETRACTORSimpson/Basye, Inc.K892693VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTZinnanti Surgical Instruments, Inc.K891035NEEDLE EXTENSIONSZinnanti Surgical Instruments, Inc.K891049ZEPPELIN SCISSORSZinnanti Surgical Instruments, 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.

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