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FDA 510(k)

MASTER KIT B

K-Number: K861142 · 1986-07-10

ApplicantPro-Lab, Inc.
Decision Date1986-07-10
Product CodeLRP
Advisory CommitteeSU
DecisionUnknown

Device Summary

MASTER KIT B is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab, Inc.. It received FDA 510(k) clearance on 1986-07-10 under 510(k) number K861142. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MASTER KIT B?

MASTER KIT B is a medical device that received FDA 510(k) clearance on 1986-07-10. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K861142.

When did MASTER KIT B receive FDA 510(k) clearance?

MASTER KIT B received FDA 510(k) clearance on 1986-07-10, under 510(k) number K861142.

Who is the listed applicant for MASTER KIT B?

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

What is the FDA product code for MASTER KIT B?

The FDA product code for MASTER KIT B is LRP.

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Other records listing Pro-Lab, Inc. as applicant

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Related Devices (Code: LRP)

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.

K963723LACERATION TRAYGrand Medical ProductsK951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical Products

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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