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FDA 510(k)

PAN-AM MYELOGRAM TRAY

K-Number: K801431 · 1980-08-12

ApplicantWaters Assoc., Inc.
Decision Date1980-08-12
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAN-AM MYELOGRAM TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Waters Assoc., Inc.. It received FDA 510(k) clearance on 1980-08-12 under 510(k) number K801431. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAN-AM MYELOGRAM TRAY?

PAN-AM MYELOGRAM TRAY is a medical device that received FDA 510(k) clearance on 1980-08-12. The listed applicant is Waters Assoc., Inc.. The 510(k) number is K801431.

When did PAN-AM MYELOGRAM TRAY receive FDA 510(k) clearance?

PAN-AM MYELOGRAM TRAY received FDA 510(k) clearance on 1980-08-12, under 510(k) number K801431.

Who is the listed applicant for PAN-AM MYELOGRAM TRAY?

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

What is the FDA product code for PAN-AM MYELOGRAM TRAY?

The FDA product code for PAN-AM MYELOGRAM TRAY is FMI.

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Related Devices (Code: FMI)

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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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