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FDA 510(k)

INJECT-R FILL

K-Number: K931742 · 1993-05-27

ApplicantUnion Broach, Div. Moyco Industries, Inc.
Decision Date1993-05-27
Product CodeEKM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INJECT-R FILL is the device name listed in this FDA 510(k) record. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. It received FDA 510(k) clearance on 1993-05-27 under 510(k) number K931742. The device is classified under product code EKM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECT-R FILL?

INJECT-R FILL is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. The 510(k) number is K931742.

When did INJECT-R FILL receive FDA 510(k) clearance?

INJECT-R FILL received FDA 510(k) clearance on 1993-05-27, under 510(k) number K931742.

Who is the listed applicant for INJECT-R FILL?

The FDA 510(k) record lists Union Broach, Div. Moyco Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECT-R FILL?

The FDA product code for INJECT-R FILL is EKM.

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Other records listing Union Broach, Div. Moyco Industries, 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.

K962733CYBER-FIL ALKENOATE CEMENT MULTI-PURPOSE KIT (23900/23905/23910/23915/23920)K950365MOYCO-EDTAK941574RETRO MIRRORK940260THERMAL PULP TESTERK935542NICKEL-TITANIUM K-TYPE FILEK923661QUADRASORB FILTER

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Related Devices (Code: EKM)

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.

K073369EI DOWNPAK BARRIER SLEEVESHu-Friedy Mfg. Co., Inc.K070246DOWN PAKEndo Twinn B.V.K051573TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)Dr. Howard Martin, P.A.K042870ENDO TWINNEndo Twinn B.V.K023819FIBERFILL SGPPentron Clinical TechnologiesK971641ANTIBACTERIAL GUTTA PERCHADr. Howard Martin, P.A.

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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