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FDA 510(k)

CIRCUMCISION TRAY

K-Number: K935697 · 1994-05-02

ApplicantCush Medical Products
Decision Date1994-05-02
Product CodeHFX
Advisory CommitteeOB
DecisionUnknown

Device Summary

CIRCUMCISION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Cush Medical Products. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K935697. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CIRCUMCISION TRAY?

CIRCUMCISION TRAY is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Cush Medical Products. The 510(k) number is K935697.

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

CIRCUMCISION TRAY received FDA 510(k) clearance on 1994-05-02, under 510(k) number K935697.

Who is the listed applicant for CIRCUMCISION TRAY?

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

What is the FDA product code for CIRCUMCISION TRAY?

The FDA product code for CIRCUMCISION TRAY is HFX.

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Other records listing Cush Medical Products 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.

K943424CUSH ISLAND DRESSINGK940518C-SECTION TRAYK941349DENTAL TRAYK941645BIOPSY TRAYK940239EYE TRAYK935684IV START KIT

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Related Devices (Code: HFX)

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.

K251687Konig Bell Circumcision ClampMedline Industries, LPK221356Wee BellWee MedicalK212911Konig Mogen ClampMedline Industries, Inc.K131373SHANGRINGWuhu Snnda Medical Treatment Appliance TechnologyK121789SHANGRINGWuhu Snna Medical Treatment Appliance Technology CK103695PREPEX SYSTEMCirc Medtech

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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