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FDA 510(k)

ENDOMARK STERILE INDIA INK

K-Number: K042901 · 2005-03-16

ApplicantPmt Corp.
Decision Date2005-03-16
Product CodeNBG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOMARK STERILE INDIA INK is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 2005-03-16 under 510(k) number K042901. The device is classified under product code NBG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOMARK STERILE INDIA INK?

ENDOMARK STERILE INDIA INK is a medical device that received FDA 510(k) clearance on 2005-03-16. The listed applicant is Pmt Corp.. The 510(k) number is K042901.

When did ENDOMARK STERILE INDIA INK receive FDA 510(k) clearance?

ENDOMARK STERILE INDIA INK received FDA 510(k) clearance on 2005-03-16, under 510(k) number K042901.

Who is the listed applicant for ENDOMARK STERILE INDIA INK?

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

What is the FDA product code for ENDOMARK STERILE INDIA INK?

The FDA product code for ENDOMARK STERILE INDIA INK is NBG.

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Other records listing Pmt Corp. as applicant

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Related Devices (Code: NBG)

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.

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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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