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FDA 510(k)

FRAY BIO-PUNCH

K-Number: K921822 · 1992-10-28

ApplicantFray Products Corp.
Decision Date1992-10-28
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FRAY BIO-PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Fray Products Corp.. It received FDA 510(k) clearance on 1992-10-28 under 510(k) number K921822. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAY BIO-PUNCH?

FRAY BIO-PUNCH is a medical device that received FDA 510(k) clearance on 1992-10-28. The listed applicant is Fray Products Corp.. The 510(k) number is K921822.

When did FRAY BIO-PUNCH receive FDA 510(k) clearance?

FRAY BIO-PUNCH received FDA 510(k) clearance on 1992-10-28, under 510(k) number K921822.

Who is the listed applicant for FRAY BIO-PUNCH?

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

What is the FDA product code for FRAY BIO-PUNCH?

The FDA product code for FRAY BIO-PUNCH is MDM.

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Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, 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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