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FDA 510(k)

MINIGARD DISPOSABLE LINERS

K-Number: K840755 · 1984-04-13

ApplicantIpco Corp.
Decision Date1984-04-13
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINIGARD DISPOSABLE LINERS is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840755. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIGARD DISPOSABLE LINERS?

MINIGARD DISPOSABLE LINERS is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Ipco Corp.. The 510(k) number is K840755.

When did MINIGARD DISPOSABLE LINERS receive FDA 510(k) clearance?

MINIGARD DISPOSABLE LINERS received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840755.

Who is the listed applicant for MINIGARD DISPOSABLE LINERS?

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

What is the FDA product code for MINIGARD DISPOSABLE LINERS?

The FDA product code for MINIGARD DISPOSABLE LINERS is EYQ.

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 Ipco Corp. 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 23 devices →

Related Devices (Code: EYQ)

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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