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FDA 510(k)

JAIN QUICK COUNT

K-Number: K911076 · 1991-05-30

ApplicantJain Surgical Equipment, Inc.
Decision Date1991-05-30
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JAIN QUICK COUNT is the device name listed in this FDA 510(k) record. The listed applicant is Jain Surgical Equipment, Inc.. It received FDA 510(k) clearance on 1991-05-30 under 510(k) number K911076. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAIN QUICK COUNT?

JAIN QUICK COUNT is a medical device that received FDA 510(k) clearance on 1991-05-30. The listed applicant is Jain Surgical Equipment, Inc.. The 510(k) number is K911076.

When did JAIN QUICK COUNT receive FDA 510(k) clearance?

JAIN QUICK COUNT received FDA 510(k) clearance on 1991-05-30, under 510(k) number K911076.

Who is the listed applicant for JAIN QUICK COUNT?

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

What is the FDA product code for JAIN QUICK COUNT?

The FDA product code for JAIN QUICK COUNT is MMK.

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.

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Other records listing Jain Surgical Equipment, 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.

K913896JAIN BLOOD SHIELDK911077JAIN SUTURE PACKAGE COUNTERK905105JAIN SUTURE/VESIBAND ORGANIZERK904536JAIN GRAFT ASSIST

Related Devices (Code: MMK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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