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FDA 510(k)

R & D BATTERIES, INC. PART NUMBER 5113

K-Number: K935244 · 1994-04-19

ApplicantR & D Batteries, Inc.
Decision Date1994-04-19
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

R & D BATTERIES, INC. PART NUMBER 5113 is the device name listed in this FDA 510(k) record. The listed applicant is R & D Batteries, Inc.. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K935244. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R & D BATTERIES, INC. PART NUMBER 5113?

R & D BATTERIES, INC. PART NUMBER 5113 is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K935244.

When did R & D BATTERIES, INC. PART NUMBER 5113 receive FDA 510(k) clearance?

R & D BATTERIES, INC. PART NUMBER 5113 received FDA 510(k) clearance on 1994-04-19, under 510(k) number K935244.

Who is the listed applicant for R & D BATTERIES, INC. PART NUMBER 5113?

The FDA 510(k) record lists R & D Batteries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R & D BATTERIES, INC. PART NUMBER 5113?

The FDA product code for R & D BATTERIES, INC. PART NUMBER 5113 is ILQ.

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Other records listing R & D Batteries, 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.

K951284R&D BATTERIES, INC. PART NUMBERS 5137, 5140, 5142 AND 5155K951277R&D BATTERIES, INC. PART NUMBERS 5295, 5334, 5344 AND 5410K951278R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284K951280R&D BATTERIES, INC. PART NUMBERS 5003, 5006, 5008 AND 5012K951285R&D BATTERIES, INC. PART NUMBERS 5158, 5168, 5171 AND 5172K951276R&D BATTERIES, INC. PART NUMBERS 5412, 5420, 5436 AND 5438

View all 52 devices →

Related Devices (Code: ILQ)

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.

K162817Noddle(TM)Iowa Adaptive Technologies, Inc. Dba Voxello, Inc.K943035P.A.T. SYSTEMMathews Assoc., Inc.K930044COMFORT KEYBOARD SYSTEMHealth Care Keyboard Co., Inc.K931855LIGHTWRITERZygo Corp.K935981MLT-2Med Labs, Inc.K925387LIBERATORPrentke Romich Co.

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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