FDA 510(k)

HSG TRAY

K-Number: K920803 · 1992-10-19

Decision Date1992-10-19

Product CodeHIB

Advisory CommitteeOB

DecisionUnknown

Device Summary

HSG TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Unimar, Inc.. It received FDA 510(k) clearance on 1992-10-19 under 510(k) number K920803. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HSG TRAY?

HSG TRAY is a medical device that received FDA 510(k) clearance on 1992-10-19. The listed applicant is Unimar, Inc.. The 510(k) number is K920803.

When did HSG TRAY receive FDA 510(k) clearance?

HSG TRAY received FDA 510(k) clearance on 1992-10-19, under 510(k) number K920803.

Who is the listed applicant for HSG TRAY?

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

What is the FDA product code for HSG TRAY?

The FDA product code for HSG TRAY is HIB.

Other records listing Unimar, 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.

K932432KRONNER REINFORCING STYLETTE K910317UNI-SEM(TM)K904473KRONNER MANIPUJECTOR K895659HUI MINI-FLEX K895403ASPIRETTE ENDOCERVICAL ASPIRATOR K894264KDF-2.3

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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.