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FDA 510(k)

TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS

K-Number: K951703 · 1995-06-28

ApplicantProducts For Medicine
Decision Date1995-06-28
Product CodeLRT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS is the device name listed in this FDA 510(k) record. The listed applicant is Products For Medicine. It received FDA 510(k) clearance on 1995-06-28 under 510(k) number K951703. The device is classified under product code LRT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS?

TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS is a medical device that received FDA 510(k) clearance on 1995-06-28. The listed applicant is Products For Medicine. The 510(k) number is K951703.

When did TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS receive FDA 510(k) clearance?

TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS received FDA 510(k) clearance on 1995-06-28, under 510(k) number K951703.

Who is the listed applicant for TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS?

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

What is the FDA product code for TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS?

The FDA product code for TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS is LRT.

Related Clinical Trials

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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Other records listing Products For Medicine 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.

K963227WHITE SUN LIGHT SOURCE MODEL #: XL300 AND #: XL175K955510X6000D SILENT SUN LIGHT SOURCEK953089I-SPOUSEK951704NON-WOVEN FILTER PAPER FOR STEAM AND GAS STERILIZATIONK883658I-SPOSE EYE SHIELD

Related Devices (Code: LRT)

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.

K002937TST CONTROL INTEGRATOR FOR STEAM STERILIZERSAlbert Browne , Ltd.K965154TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVEAlbert Browne , Ltd.K951113CROSS-CHECKSSteritec Products Mfg Co, Inc.K871672STERILIZATION INDICATOR FOR FLASH STERILIZATIONPropper Mfg. Co., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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