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FDA 510(k)

MEDLINE CIRCUMCISION TRAY

K-Number: K970282 · 1997-03-06

ApplicantMedline
Decision Date1997-03-06
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDLINE CIRCUMCISION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medline. It received FDA 510(k) clearance on 1997-03-06 under 510(k) number K970282. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE CIRCUMCISION TRAY?

MEDLINE CIRCUMCISION TRAY is a medical device that received FDA 510(k) clearance on 1997-03-06. The listed applicant is Medline. The 510(k) number is K970282.

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

MEDLINE CIRCUMCISION TRAY received FDA 510(k) clearance on 1997-03-06, under 510(k) number K970282.

Who is the listed applicant for MEDLINE CIRCUMCISION TRAY?

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

What is the FDA product code for MEDLINE CIRCUMCISION TRAY?

The FDA product code for MEDLINE CIRCUMCISION TRAY is HFX.

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Other records listing Medline 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.

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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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