FDA 510(k)

G.E. STERILE AMNIOCENTESIS TRAY

K-Number: K960203 · 1996-03-14

Decision Date1996-03-14

Product CodeHIO

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

G.E. STERILE AMNIOCENTESIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1996-03-14 under 510(k) number K960203. The device is classified under product code HIO. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. STERILE AMNIOCENTESIS TRAY?

G.E. STERILE AMNIOCENTESIS TRAY is a medical device that received FDA 510(k) clearance on 1996-03-14. The listed applicant is GE Medical Systems. The 510(k) number is K960203.

When did G.E. STERILE AMNIOCENTESIS TRAY receive FDA 510(k) clearance?

G.E. STERILE AMNIOCENTESIS TRAY received FDA 510(k) clearance on 1996-03-14, under 510(k) number K960203.

Who is the listed applicant for G.E. STERILE AMNIOCENTESIS TRAY?

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

What is the FDA product code for G.E. STERILE AMNIOCENTESIS TRAY?

The FDA product code for G.E. STERILE AMNIOCENTESIS TRAY is HIO.

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Related Devices (Code: HIO)

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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.