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FDA 510(k)

PERAMBULATOR (STROLLER)

K-Number: K862888 · 1986-08-13

ApplicantMednet, Inc.
Decision Date1986-08-13
Product CodeLBE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERAMBULATOR (STROLLER) is the device name listed in this FDA 510(k) record. The listed applicant is Mednet, Inc.. It received FDA 510(k) clearance on 1986-08-13 under 510(k) number K862888. The device is classified under product code LBE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERAMBULATOR (STROLLER)?

PERAMBULATOR (STROLLER) is a medical device that received FDA 510(k) clearance on 1986-08-13. The listed applicant is Mednet, Inc.. The 510(k) number is K862888.

When did PERAMBULATOR (STROLLER) receive FDA 510(k) clearance?

PERAMBULATOR (STROLLER) received FDA 510(k) clearance on 1986-08-13, under 510(k) number K862888.

Who is the listed applicant for PERAMBULATOR (STROLLER)?

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

What is the FDA product code for PERAMBULATOR (STROLLER)?

The FDA product code for PERAMBULATOR (STROLLER) is LBE.

Related Clinical Trials

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.

Other records listing Mednet, 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.

View all 12 devices →

Related Devices (Code: LBE)

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.

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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