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FDA 510(k)

MACLEAN-FOGG, DISPOS-INOCULA-LOOPS

K-Number: K842057 · 1984-06-07

ApplicantPolymer Technology Corp.
Decision Date1984-06-07
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MACLEAN-FOGG, DISPOS-INOCULA-LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Corp.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K842057. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACLEAN-FOGG, DISPOS-INOCULA-LOOPS?

MACLEAN-FOGG, DISPOS-INOCULA-LOOPS is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Polymer Technology Corp.. The 510(k) number is K842057.

When did MACLEAN-FOGG, DISPOS-INOCULA-LOOPS receive FDA 510(k) clearance?

MACLEAN-FOGG, DISPOS-INOCULA-LOOPS received FDA 510(k) clearance on 1984-06-07, under 510(k) number K842057.

Who is the listed applicant for MACLEAN-FOGG, DISPOS-INOCULA-LOOPS?

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

What is the FDA product code for MACLEAN-FOGG, DISPOS-INOCULA-LOOPS?

The FDA product code for MACLEAN-FOGG, DISPOS-INOCULA-LOOPS is LIB.

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Related Devices (Code: LIB)

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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