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FDA 510(k)

MEDSURG AMNIOCENTESIS TRAY

K-Number: K854290 · 1986-01-24

ApplicantMedsurg Industries, Inc.
Decision Date1986-01-24
Product Code
DecisionUnknown

Device Summary

MEDSURG AMNIOCENTESIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K854290. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDSURG AMNIOCENTESIS TRAY?

MEDSURG AMNIOCENTESIS TRAY is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K854290.

When did MEDSURG AMNIOCENTESIS TRAY receive FDA 510(k) clearance?

MEDSURG AMNIOCENTESIS TRAY received FDA 510(k) clearance on 1986-01-24, under 510(k) number K854290.

Who is the listed applicant for MEDSURG AMNIOCENTESIS TRAY?

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

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Other records listing Medsurg Industries, 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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

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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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